A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981959



Internal ID18617155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85275237..85275737hg38UCSC Ensembl
Innerchr8:86187466..86187966hg19UCSC Ensembl
Innerchr8:86374718..86375218hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2510836, nssv2510838, nssv2510835, nssv2510833, nssv2510831, nssv2510837, nssv2510834, nssv2510832, nssv2510839, nssv2510840
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCA13
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981959
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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