A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518025



Internal ID15098632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32398293..32415706hg38UCSC Ensembl
Innerchr3:32439785..32457198hg19UCSC Ensembl
Innerchr3:32414789..32432202hg18UCSC Ensembl
Innerchr3:32414789..32432202hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3817414
hg1917414
hg1817414
hg1717414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695435
Samples
Known GenesCMTM7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518025
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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