A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523771



Internal ID15451064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82314045..82363543hg38UCSC Ensembl
Innerchr3:82363196..82412694hg19UCSC Ensembl
Innerchr3:82445886..82495384hg18UCSC Ensembl
Innerchr3:82445886..82495384hg17UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3849499
hg1949499
hg1849499
hg1749499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699593
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523771
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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