A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979436



Internal ID18614639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47821901..47850111hg38UCSC Ensembl
Innerchr20:46450645..46478855hg19UCSC Ensembl
Innerchr20:45884052..45912262hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3828211
hg1928211
hg1828211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2238492, nssv2238490, nssv2238493, nssv2238495, nssv2238494, nssv2238489, nssv2238487, nssv2238486, nssv2238491, nssv2238488
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)nsv979436
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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