A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967095



Internal ID18602324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179463821..179466478hg38UCSC Ensembl
Innerchr3:179181609..179184266hg19UCSC Ensembl
Innerchr3:180664303..180666960hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg382658
hg192658
hg182658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2305232, nssv2305237, nssv2305239, nssv2305240, nssv2305234, nssv2305238, nssv2305235, nssv2305236, nssv2305233, nssv2305241
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967095
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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