A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151784



Internal ID19196575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:67889071..67895272hg38UCSC Ensembl
Outerchr5:67184899..67191100hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg386202
hg196202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998964
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151784
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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