A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984079



Internal ID18619269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59524308..59530995hg38UCSC Ensembl
Innerchr15:59816507..59823194hg19UCSC Ensembl
Innerchr15:57603799..57610486hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg386688
hg196688
hg186688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2026074, nssv2026076, nssv2026072, nssv2026069, nssv2026071, nssv2026068, nssv2026073, nssv2026067, nssv2026070, nssv2026075
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)nsv984079
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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