A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999650



Internal ID18843050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110208174..110220275hg38UCSC Ensembl
Outerchr11:110078899..110091000hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3812102
hg1912102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152468
Supporting Variants
SamplesKWB1
Known GenesRDX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999650
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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