A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965191



Internal ID18600425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98468851..98470407hg38UCSC Ensembl
Innerchr3:98187695..98189251hg19UCSC Ensembl
Innerchr3:99670385..99671941hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381557
hg191557
hg181557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2286881, nssv2286876, nssv2286875, nssv2286877, nssv2286879, nssv2286880, nssv2286874, nssv2286883, nssv2286882, nssv2286878
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR5K1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965191
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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