A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525132



Internal ID15452425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36732343..36737608hg38UCSC Ensembl
Innerchr2:36959486..36964751hg19UCSC Ensembl
Innerchr2:36812990..36818255hg18UCSC Ensembl
Innerchr2:36871137..36876402hg17UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg385266
hg195266
hg185266
hg175266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701200
Samples
Known GenesVIT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525132
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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