A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965158



Internal ID18600392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37789104..37790274hg38UCSC Ensembl
Innerchr3:37830595..37831765hg19UCSC Ensembl
Innerchr3:37805599..37806769hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381171
hg191171
hg181171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2279184, nssv2279191, nssv2279189, nssv2279185, nssv2279192, nssv2279190, nssv2279183, nssv2279188, nssv2279187, nssv2279186
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesITGA9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965158
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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