A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973322



Internal ID18608537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63057897..63058397hg38UCSC Ensembl
Innerchr9:66962869..66963369hg19UCSC Ensembl
Innerchr9:66702689..66703189hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2736855, nssv2736857, nssv2736851, nssv2736859, nssv2736854, nssv2736852, nssv2736850, nssv2736858, nssv2736856, nssv2736853
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973322
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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