A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965857



Internal ID18601087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17600455..17600955hg38UCSC Ensembl
Innerchr20:17581100..17581600hg19UCSC Ensembl
Innerchr20:17529100..17529600hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2230045, nssv2230038, nssv2230047, nssv2230040, nssv2230042, nssv2230039, nssv2230044, nssv2230046, nssv2230043, nssv2230041
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDSTN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965857
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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