A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972082



Internal ID18607298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124021856..124024099hg38UCSC Ensembl
Innerchr11:123892563..123894806hg19UCSC Ensembl
Innerchr11:123397773..123400016hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382244
hg192244
hg182244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1907147, nssv1907142, nssv1907140, nssv1907145, nssv1907139, nssv1907138, nssv1907141, nssv1907146, nssv1907144, nssv1907143
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR10G9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972082
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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