A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519232



Internal ID15446525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35965622..35977275hg38UCSC Ensembl
Innerchr3:36007114..36018767hg19UCSC Ensembl
Innerchr3:35982118..35993771hg18UCSC Ensembl
Innerchr3:35982118..35993771hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3811654
hg1911654
hg1811654
hg1711654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv280n21
Supporting Variantsnssv696724
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519232
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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