A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972003



Internal ID18607219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43134125..43145538hg38UCSC Ensembl
Innerchr11:43155675..43167088hg19UCSC Ensembl
Innerchr11:43112251..43123664hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3811414
hg1911414
hg1811414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1882307, nssv1882308, nssv1882306, nssv1882305, nssv1882312, nssv1882304, nssv1882310, nssv1882313, nssv1882311, nssv1882309
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)nsv972003
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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