A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520634



Internal ID15447927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6979775..6983663hg38UCSC Ensembl
Innerchr11:7001006..7004894hg19UCSC Ensembl
Innerchr11:6957582..6961470hg18UCSC Ensembl
Innerchr11:6957582..6961470hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383889
hg193889
hg183889
hg173889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685659, nssv673391
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520634
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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