A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700772



Internal ID15437424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89494527..89548529hg38UCSC Ensembl
Innerchr3:89543677..89597679hg19UCSC Ensembl
Innerchr3:89626367..89680369hg18UCSC Ensembl
Innerchr3:89626367..89680369hg17UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3854003
hg1954003
hg1854003
hg1754003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524781
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700772
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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