A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523926



Internal ID15451219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119010267..119083007hg38UCSC Ensembl
Innerchr3:118729114..118801854hg19UCSC Ensembl
Innerchr3:120211804..120284544hg18UCSC Ensembl
Innerchr3:120211804..120284544hg17UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3872741
hg1972741
hg1872741
hg1772741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699771
Samples
Known GenesIGSF11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523926
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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