A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972394



Internal ID18607610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65770735..65846000hg38UCSC Ensembl
Innerchr9:70318730..70395310hg19UCSC Ensembl
Innerchr9:69558373..69635130hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3875266
hg1976581
hg1876758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2550857, nssv2550861, nssv2550855, nssv2550862, nssv2550858, nssv2550863, nssv2550860, nssv2550854, nssv2550859, nssv2550856
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)nsv972394
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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