A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673010



Internal ID15409662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159138994..159151890hg38UCSC Ensembl
Innerchr6:159560026..159572922hg19UCSC Ensembl
Innerchr6:159480014..159492910hg18UCSC Ensembl
Innerchr6:159530435..159543331hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3812897
hg1912897
hg1812897
hg1712897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519356
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673010
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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