A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520292



Internal ID15447585
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 StatusM
Merged Variants
Supporting Variantsnssv697331
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520292
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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