A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525269



Internal ID15452562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:206718682..206726333hg38UCSC Ensembl
Innerchr2:207583406..207591057hg19UCSC Ensembl
Innerchr2:207291651..207299302hg18UCSC Ensembl
Innerchr2:207408912..207416563hg17UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg387652
hg197652
hg187652
hg177652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701369
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525269
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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