A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965971



Internal ID18601201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13803362..14001586hg38UCSC Ensembl
Innerchr21:15175683..15373907hg19UCSC Ensembl
Innerchr21:14097554..14295778hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38198225
hg19198225
hg18198225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2244246, nssv2244239, nssv2244244, nssv2244245, nssv2244241, nssv2244238, nssv2244237, nssv2244242, nssv2244243, nssv2244240
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A11P, C21orf15
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965971
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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