A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965887



Internal ID18601117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53743028..53749426hg38UCSC Ensembl
Innerchr20:52359567..52365965hg19UCSC Ensembl
Innerchr20:51792974..51799372hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386399
hg196399
hg186399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2239484, nssv2239478, nssv2239483, nssv2239482, nssv2239479, nssv2239480, nssv2239481, nssv2239475, nssv2239476, nssv2239477
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)nsv965887
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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