A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526638



Internal ID15453931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22669766..22674843hg38UCSC Ensembl
Innerchr2:22892638..22897715hg19UCSC Ensembl
Innerchr2:22746143..22751220hg18UCSC Ensembl
Innerchr2:22804290..22809367hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg385078
hg195078
hg185078
hg175078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702960
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526638
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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