A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967010



Internal ID18602239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44707118..44710555hg38UCSC Ensembl
Innerchr3:44748610..44752047hg19UCSC Ensembl
Innerchr3:44723614..44727051hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383438
hg193438
hg183438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2279582, nssv2279584, nssv2279587, nssv2279589, nssv2279583, nssv2279581, nssv2279586, nssv2279580, nssv2279585, nssv2279588
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)nsv967010
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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