A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965978



Internal ID18601208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26234078..26235394hg38UCSC Ensembl
Innerchr21:27606397..27607713hg19UCSC Ensembl
Innerchr21:26528268..26529584hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg381317
hg191317
hg181317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2245395, nssv2245394, nssv2245397, nssv2245398, nssv2245389, nssv2245396, nssv2245392, nssv2245393, nssv2245390, nssv2245391
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)nsv965978
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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