A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523837



Internal ID15451130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119560001..119570001hg38UCSC Ensembl
Innerchr3:119278848..119288848hg19UCSC Ensembl
Innerchr3:120761538..120771538hg18UCSC Ensembl
Innerchr3:120761538..120771538hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3810001
hg1910001
hg1810001
hg1710001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699669
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523837
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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