A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527220



Internal ID15454513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101720460..101739649hg38UCSC Ensembl
Innerchr11:101591191..101610380hg19UCSC Ensembl
Innerchr11:101096401..101115590hg18UCSC Ensembl
Innerchr11:101096401..101115590hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3819190
hg1919190
hg1819190
hg1719190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703620
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527220
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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