A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975968



Internal ID18611175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93858244..93864033hg38UCSC Ensembl
Innerchr11:93591410..93597199hg19UCSC Ensembl
Innerchr11:93231058..93236847hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385790
hg195790
hg185790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901803, nssv1901802, nssv1901806, nssv1901808, nssv1901809, nssv1901807, nssv1901810, nssv1901801, nssv1901805, nssv1901804
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)nsv975968
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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