A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965882



Internal ID18601112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:49802815..49806753hg38UCSC Ensembl
Innerchr20:48419352..48423290hg19UCSC Ensembl
Innerchr20:47852759..47856697hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg383939
hg193939
hg183939
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2238736, nssv2238733, nssv2238728, nssv2238729, nssv2238730, nssv2238735, nssv2238737, nssv2238732, nssv2238731, nssv2238734
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)nsv965882
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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