A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965856



Internal ID18601086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17188283..17190113hg38UCSC Ensembl
Innerchr20:17168928..17170758hg19UCSC Ensembl
Innerchr20:17116928..17118758hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381831
hg191831
hg181831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2229324, nssv2229323, nssv2229318, nssv2229317, nssv2229316, nssv2229320, nssv2229325, nssv2229319, nssv2229321, nssv2229322
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)nsv965856
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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