A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686457



Internal ID15423109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29376927..29384096hg38UCSC Ensembl
Innerchr6:29344704..29351873hg19UCSC Ensembl
Innerchr6:29452683..29459852hg18UCSC Ensembl
Innerchr6:29452683..29459852hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg387170
hg197170
hg187170
hg177170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519453
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686457
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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