A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684657



Internal ID15421309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4379088..4379656hg38UCSC Ensembl
Innerchr7:4418719..4419287hg19UCSC Ensembl
Innerchr7:4385245..4385813hg18UCSC Ensembl
Innerchr7:4191960..4192528hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38569
hg19569
hg18569
hg17569
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517675
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684657
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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