A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968669



Internal ID18603897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62687316..62687971hg38UCSC Ensembl
Innerchr9:46998617..46999272hg19UCSC Ensembl
Innerchr9:46838437..46839092hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg38656
hg19656
hg18656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2544509, nssv2544517, nssv2544512, nssv2544510, nssv2544513, nssv2544514, nssv2544515, nssv2544516, nssv2544511, nssv2544508
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)nsv968669
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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