A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701203



Internal ID15437855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146955801..146965885hg38UCSC Ensembl
Innerchr3:146673588..146683672hg19UCSC Ensembl
Innerchr3:148156278..148166362hg18UCSC Ensembl
Innerchr3:148156286..148166370hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3810085
hg1910085
hg1810085
hg1710085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516386
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701203
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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