A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671093



Internal ID15407745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176178790..176219995hg38UCSC Ensembl
Innerchr3:175896578..175937783hg19UCSC Ensembl
Innerchr3:177379272..177420477hg18UCSC Ensembl
Innerchr3:177379280..177420485hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3841206
hg1941206
hg1841206
hg1741206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516429
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671093
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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