A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686028



Internal ID15422680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21602321..21658650hg38UCSC Ensembl
Innerchr6:21602552..21658881hg19UCSC Ensembl
Innerchr6:21710531..21766860hg18UCSC Ensembl
Innerchr6:21710531..21766860hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3856330
hg1956330
hg1856330
hg1756330
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519363
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686028
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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