A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971666



Internal ID18606883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73904959..73914679hg38UCSC Ensembl
Innerchr8:74817194..74826914hg19UCSC Ensembl
Innerchr8:74979748..74989468hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg389721
hg199721
hg189721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2506876, nssv2506875, nssv2506877, nssv2506874, nssv2506870, nssv2506873, nssv2506872, nssv2506879, nssv2506878, nssv2506871
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)nsv971666
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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