A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665570



Internal ID15055536
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515978
Supporting Variants
Samples
Known GenesC7orf26, GRID2IP, ZDHHC4, ZNF316, ZNF853
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665570
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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