A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965876



Internal ID18601106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:43650198..43654189hg38UCSC Ensembl
Innerchr20:42278838..42282829hg19UCSC Ensembl
Innerchr20:41712252..41716243hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg383992
hg193992
hg183992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2237353, nssv2237357, nssv2237360, nssv2237362, nssv2237361, nssv2237354, nssv2237358, nssv2237359, nssv2237356, nssv2237355
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)nsv965876
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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