A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653127



Internal ID15043093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94706013..94777433hg38UCSC Ensembl
Innerchr6:95415731..95487151hg19UCSC Ensembl
Innerchr6:95472452..95543872hg18UCSC Ensembl
Innerchr6:95472452..95543872hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3871421
hg1971421
hg1871421
hg1771421
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653127
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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