A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699517



Internal ID15089483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6573973..6650609hg38UCSC Ensembl
Innerchr7:6613604..6690240hg19UCSC Ensembl
Innerchr7:6580129..6656765hg18UCSC Ensembl
Innerchr7:6386844..6463480hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3876637
hg1976637
hg1876637
hg1776637
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515978
Supporting Variants
Samples
Known GenesC7orf26, ZDHHC4, ZNF316, ZNF853
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699517
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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