A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972079



Internal ID18607295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118827987..118834543hg38UCSC Ensembl
Innerchr11:118698696..118705252hg19UCSC Ensembl
Innerchr11:118203906..118210462hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386557
hg196557
hg186557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1906363, nssv1906369, nssv1906371, nssv1906368, nssv1906366, nssv1906364, nssv1906367, nssv1906370, nssv1906372, nssv1906365
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)nsv972079
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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