A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975987



Internal ID18611194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121361062..121362894hg38UCSC Ensembl
Innerchr11:121231771..121233603hg19UCSC Ensembl
Innerchr11:120736981..120738813hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381833
hg191833
hg181833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1903868, nssv1903864, nssv1903863, nssv1903871, nssv1903865, nssv1903869, nssv1903870, nssv1903866, nssv1903862, nssv1903867
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)nsv975987
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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