A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962579



Internal ID18597822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37528387..37532096hg38UCSC Ensembl
Innerchr20:36156789..36160498hg19UCSC Ensembl
Innerchr20:35590203..35593912hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383710
hg193710
hg183710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2235970, nssv2235961, nssv2235962, nssv2235968, nssv2235963, nssv2235965, nssv2235966, nssv2235967, nssv2235969, nssv2235964
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)nsv962579
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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