A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525881



Internal ID15453174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116384741..116417192hg38UCSC Ensembl
Innerchr11:116255458..116287909hg19UCSC Ensembl
Innerchr11:115760668..115793119hg18UCSC Ensembl
Innerchr11:115760668..115793119hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3832452
hg1932452
hg1832452
hg1732452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702081
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525881
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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