A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967547



Internal ID18602775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67190..70989hg38UCSC Ensembl
Innerchr8:17190..20989hg19UCSC Ensembl
Innerchr8:7190..10989hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg383800
hg193800
hg183800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2488840, nssv2488841, nssv2488839, nssv2488836, nssv2488843, nssv2488838, nssv2488844, nssv2488842, nssv2488837, nssv2488845
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)nsv967547
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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