A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964381



Internal ID18252933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23634168..23641209hg38UCSC Ensembl
Innerchr20:23614805..23621846hg19UCSC Ensembl
Innerchr20:23562805..23569846hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg387042
hg197042
hg187042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2231255, nssv2231257, nssv2231258, nssv2231254, nssv2231259, nssv2231252, nssv2231260, nssv2231256, nssv2231253, nssv2231261
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCST3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964381
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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