A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965879



Internal ID18601109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45815184..45815989hg38UCSC Ensembl
Innerchr20:44443823..44444628hg19UCSC Ensembl
Innerchr20:43877230..43878035hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38806
hg19806
hg18806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2238173, nssv2238180, nssv2238174, nssv2238179, nssv2238172, nssv2238176, nssv2238175, nssv2238178, nssv2238177, nssv2238181
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesUBE2C
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965879
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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