A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697331



Internal ID15433983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163753585..163769887hg38UCSC Ensembl
Innerchr6:164174617..164190919hg19UCSC Ensembl
Innerchr6:164094607..164110909hg18UCSC Ensembl
Innerchr6:164145028..164161330hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3816303
hg1916303
hg1816303
hg1716303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520292
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697331
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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