A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704455



Internal ID15441107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98333977..98353764hg38UCSC Ensembl
Innerchr6:98781853..98801640hg19UCSC Ensembl
Innerchr6:98888574..98908361hg18UCSC Ensembl
Innerchr6:98888574..98908361hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3819788
hg1919788
hg1819788
hg1719788
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527947
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704455
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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