A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153685



Internal ID18852976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:133482904..133484205hg38UCSC Ensembl
Outerchr11:133352799..133354100hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002340
SamplesKWB1
Known GenesOPCML
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153685
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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