A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963342



Internal ID18598583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98133193..98133941hg38UCSC Ensembl
Innerchr3:97852037..97852785hg19UCSC Ensembl
Innerchr3:99334727..99335475hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38749
hg19749
hg18749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2289157, nssv2289156, nssv2289161, nssv2289159, nssv2289155, nssv2289160, nssv2289162, nssv2289154, nssv2289153, nssv2289158
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR5H1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963342
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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