A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525815



Internal ID15453108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164596840..164849406hg38UCSC Ensembl
Innerchr6:165017873..165262895hg19UCSC Ensembl
Innerchr6:164937863..165182885hg18UCSC Ensembl
Innerchr6:164988284..165233306hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38252567
hg19245023
hg18245023
hg17245023
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702000
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525815
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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