A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515978



Internal ID15096585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6495886..6659274hg38UCSC Ensembl
Innerchr7:6535517..6698905hg19UCSC Ensembl
Innerchr7:6502042..6665430hg18UCSC Ensembl
Innerchr7:6308757..6472145hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38163389
hg19163389
hg18163389
hg17163389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697665, nssv705793, nssv699517, nssv665570, nssv697664, nssv659442
Samples
Known GenesC7orf26, GRID2IP, ZDHHC4, ZNF316, ZNF853
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515978
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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