A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975983



Internal ID18611190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114928520..114930585hg38UCSC Ensembl
Innerchr11:114799240..114801305hg19UCSC Ensembl
Innerchr11:114304450..114306515hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg382066
hg192066
hg182066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1904790, nssv1904788, nssv1904786, nssv1904784, nssv1904785, nssv1904787, nssv1904789, nssv1904783, nssv1904791, nssv1904792
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)nsv975983
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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