A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695435



Internal ID15085401
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 StatusS
Merged Variantsnsv518025
Supporting Variants
Samples
Known GenesCMTM7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695435
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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