A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979533



Internal ID18614735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32612729..32623943hg38UCSC Ensembl
Innerchr21:33985039..33996253hg19UCSC Ensembl
Innerchr21:32906910..32918124hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3811215
hg1911215
hg1811215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2248543, nssv2248544, nssv2248539, nssv2248540, nssv2248545, nssv2248541, nssv2248547, nssv2248542, nssv2248546, nssv2248548
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)nsv979533
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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