A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523857



Internal ID15451150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3715286..3728985hg38UCSC Ensembl
Innerchr3:3756970..3770669hg19UCSC Ensembl
Innerchr3:3731970..3745669hg18UCSC Ensembl
Innerchr3:3731970..3745669hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3813700
hg1913700
hg1813700
hg1713700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699692
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523857
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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