A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528237



Internal ID15455530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:38270462..38305288hg38UCSC Ensembl
Innerchr3:38311953..38346779hg19UCSC Ensembl
Innerchr3:38286957..38321783hg18UCSC Ensembl
Innerchr3:38286957..38321783hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3834827
hg1934827
hg1834827
hg1734827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704799
Samples
Known GenesSLC22A13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528237
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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