A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526763



Internal ID15454056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:142607604..142660801hg38UCSC Ensembl
Innerchr2:143365173..143418370hg19UCSC Ensembl
Innerchr2:143081643..143134840hg18UCSC Ensembl
Innerchr2:143198905..143252102hg17UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3853198
hg1953198
hg1853198
hg1753198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703115
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526763
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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