A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964380



Internal ID18599618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20252071..20254457hg38UCSC Ensembl
Innerchr20:20232715..20235101hg19UCSC Ensembl
Innerchr20:20180715..20183101hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382387
hg192387
hg182387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2230670, nssv2230668, nssv2230669, nssv2230666, nssv2230665, nssv2230664, nssv2230662, nssv2230667, nssv2230663, nssv2230661
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC20orf26
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964380
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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