A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962572



Internal ID18597815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33749069..33754400hg38UCSC Ensembl
Innerchr20:32336875..32342206hg19UCSC Ensembl
Innerchr20:31800536..31805867hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg385332
hg195332
hg185332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2234433, nssv2234431, nssv2234434, nssv2234437, nssv2234432, nssv2234430, nssv2234429, nssv2234435, nssv2234436, nssv2234438
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF341
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962572
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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