A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965846



Internal ID18601076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3485031..3491033hg38UCSC Ensembl
Innerchr20:3465678..3471680hg19UCSC Ensembl
Innerchr20:3413678..3419680hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386003
hg196003
hg186003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2227202, nssv2227207, nssv2227206, nssv2227204, nssv2227209, nssv2227200, nssv2227201, nssv2227205, nssv2227203, nssv2227208
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesATRN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965846
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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