A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982187



Internal ID18617382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10001..32355hg38UCSC Ensembl
Innerchr9:10001..32355hg19UCSC Ensembl
Innerchr9:1..22355hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3822355
hg1922355
hg1822355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2519166, nssv2519162, nssv2519161, nssv2519167, nssv2519158, nssv2519159, nssv2519165, nssv2519160, nssv2519164, nssv2519163
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDDX11L5, WASH1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982187
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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