A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151420



Internal ID19195553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:20930938..20940639hg38UCSC Ensembl
Outerchr18:18510899..18520600hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg389702
hg199702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003984
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151420
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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