A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703484



Internal ID15440136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153454175..153480035hg38UCSC Ensembl
Innerchr6:153775310..153801170hg19UCSC Ensembl
Innerchr6:153817003..153842863hg18UCSC Ensembl
Innerchr6:153867424..153893284hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3825861
hg1925861
hg1825861
hg1725861
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527104
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703484
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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