A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962573



Internal ID18597816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33910967..33913258hg38UCSC Ensembl
Innerchr20:32498773..32501064hg19UCSC Ensembl
Innerchr20:31962434..31964725hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382292
hg192292
hg182292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2234528, nssv2234535, nssv2234531, nssv2234529, nssv2234533, nssv2234534, nssv2234530, nssv2234527, nssv2234526, nssv2234532
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962573
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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