A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528926



Internal ID15109533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22862630..22880191hg38UCSC Ensembl
Innerchr1:23189123..23206684hg19UCSC Ensembl
Innerchr1:23061710..23079271hg18UCSC Ensembl
Innerchr1:22934429..22951990hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3817562
hg1917562
hg1817562
hg1717562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705616
Samples
Known GenesEPHB2, MIR4253
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528926
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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