A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982435



Internal ID18617630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42967184..42972523hg38UCSC Ensembl
Innerchr9:43998596..44003935hg19UCSC Ensembl
Innerchr9:43938592..43943931hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385340
hg195340
hg185340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2734044, nssv2734047, nssv2734040, nssv2734038, nssv2734041, nssv2734043, nssv2734046, nssv2734045, nssv2734039, nssv2734042
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)nsv982435
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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