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Variant : CV161677 (GRCh38/hg38 15q24.3(chr15:77259227-77280380)x1) Homo sapiens

Symbol: CV161677
Name: GRCh38/hg38 15q24.3(chr15:77259227-77280380)x1
Condition: See cases [RCV000140611]
Clinical Significance: likely benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PEAK1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_77259227)_(77280380_?)del
NC_000015.9:g.(?_77551569)_(77572722_?)del
NC_000015.8:g.(?_75338624)_(75359777_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381577,259,227 - 77,280,380CLINVAR
GRCh371577,551,569 - 77,572,722CLINVAR
Build 361575,338,624 - 75,359,777CLINVAR
Cytogenetic Map1515q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488141
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-08-06
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.