A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526920



Internal ID15454213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:153233907..153347757hg38UCSC Ensembl
Innerchr2:154090421..154204271hg19UCSC Ensembl
Innerchr2:153798667..153912517hg18UCSC Ensembl
Innerchr2:153915929..154029779hg17UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38113851
hg19113851
hg18113851
hg17113851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703283
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526920
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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