A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968651



Internal ID18603879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42675671..42691195hg38UCSC Ensembl
Innerchr9:44352469..44368003hg19UCSC Ensembl
Innerchr9:44292465..44307999hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3815525
hg1915535
hg1815535
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2539578, nssv2539579, nssv2539571, nssv2539576, nssv2539580, nssv2539575, nssv2539573, nssv2539574, nssv2539572, nssv2539577
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)nsv968651
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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