A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972396



Internal ID18607612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65659539..65670621hg38UCSC Ensembl
Innerchr9:70495424..70506535hg19UCSC Ensembl
Innerchr9:69735244..69746489hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3811083
hg1911112
hg1811246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2552298, nssv2552289, nssv2552295, nssv2552296, nssv2552293, nssv2552291, nssv2552292, nssv2552297, nssv2552290, nssv2552294
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)nsv972396
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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