A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983071



Internal ID18618265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124028791..124031787hg38UCSC Ensembl
Innerchr11:123899498..123902494hg19UCSC Ensembl
Innerchr11:123404708..123407704hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382997
hg192997
hg182997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1907241, nssv1907238, nssv1907240, nssv1907236, nssv1907235, nssv1907237, nssv1907243, nssv1907242, nssv1907239, nssv1908036
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR10G8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983071
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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