A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964372



Internal ID18599610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4587170..4591638hg38UCSC Ensembl
Innerchr20:4567816..4572284hg19UCSC Ensembl
Innerchr20:4515816..4520284hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg384469
hg194469
hg184469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2228284, nssv2228290, nssv2228285, nssv2228291, nssv2228289, nssv2228286, nssv2228283, nssv2226716, nssv2228287, nssv2228288
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)nsv964372
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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