A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151074



Internal ID18852504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132322105..132324106hg38UCSC Ensembl
Outerchr11:132191999..132194000hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002008
SamplesKWB1
Known GenesNTM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151074
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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