A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983002



Internal ID18618196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35997154..35997962hg38UCSC Ensembl
Innerchr11:36018704..36019512hg19UCSC Ensembl
Innerchr11:35975280..35976088hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38809
hg19809
hg18809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1881674, nssv1881668, nssv1881670, nssv1881672, nssv1881671, nssv1881673, nssv1881669, nssv1881666, nssv1881667, nssv1881675
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLDLRAD3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983002
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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