A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525644



Internal ID15106251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:54619289..54675960hg38UCSC Ensembl
Innerchr3:54653316..54709987hg19UCSC Ensembl
Innerchr3:54628356..54685027hg18UCSC Ensembl
Innerchr3:54628356..54685027hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3856672
hg1956672
hg1856672
hg1756672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701798
Samples
Known GenesCACNA2D3, ESRG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525644
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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