A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965885



Internal ID18601115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53583461..53596417hg38UCSC Ensembl
Innerchr20:52200000..52212956hg19UCSC Ensembl
Innerchr20:51633407..51646363hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3812957
hg1912957
hg1812957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2239371, nssv2239367, nssv2239369, nssv2239366, nssv2239372, nssv2239368, nssv2239363, nssv2239364, nssv2239370, nssv2239365
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)nsv965885
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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