A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975980



Internal ID18264501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114551091..114562531hg38UCSC Ensembl
Innerchr11:114421813..114433253hg19UCSC Ensembl
Innerchr11:113927023..113938463hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3811441
hg1911441
hg1811441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1903587, nssv1903586, nssv1903590, nssv1903591, nssv1903588, nssv1903583, nssv1903592, nssv1903584, nssv1903589, nssv1903585
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesNXPE1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975980
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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