A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979418



Internal ID18614621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23875511..23876800hg38UCSC Ensembl
Innerchr20:23856148..23857437hg19UCSC Ensembl
Innerchr20:23804148..23805437hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381290
hg191290
hg181290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2230964, nssv2230966, nssv2230965, nssv2230959, nssv2230961, nssv2230967, nssv2230960, nssv2230963, nssv2230968, nssv2230962
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCST5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979418
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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