A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681047



Internal ID15417699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137638098..137651931hg38UCSC Ensembl
Innerchr6:137959235..137973068hg19UCSC Ensembl
Innerchr6:138000928..138014761hg18UCSC Ensembl
Innerchr6:138000928..138014761hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3813834
hg1913834
hg1813834
hg1713834
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516698
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681047
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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