A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965858



Internal ID18601088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18006038..18018638hg38UCSC Ensembl
Innerchr20:17986682..17999282hg19UCSC Ensembl
Innerchr20:17934682..17947282hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3812601
hg1912601
hg1812601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2228034, nssv2229621, nssv2229625, nssv2229622, nssv2229627, nssv2229623, nssv2228035, nssv2229624, nssv2229626, nssv2229620
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)nsv965858
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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