A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965205



Internal ID18600439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122317575..122319495hg38UCSC Ensembl
Innerchr3:122036422..122038342hg19UCSC Ensembl
Innerchr3:123519112..123521032hg18UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg381921
hg191921
hg181921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2295363, nssv2295367, nssv2295361, nssv2295362, nssv2295369, nssv2295364, nssv2295368, nssv2295366, nssv2295365, nssv2295370
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)nsv965205
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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