A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761089



Internal ID17537045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132052660..132061233hg38UCSC Ensembl
Innerchr11:131922554..131931127hg19UCSC Ensembl
Innerchr11:131427764..131436337hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg388574
hg198574
hg188574
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983214
Supporting Variants
SamplesHGDP01307
Known GenesNTM
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761089
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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