A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020623



Internal ID22082254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6251435..6342380hg38UCSC Ensembl
Outerchr5:6248975..6345521hg38UCSC Ensembl
Innerchr5:6251548..6342493hg19UCSC Ensembl
Outerchr5:6249088..6345634hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3896547
hg1996547
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156306
Supporting Variants
Samples
Known GenesFLJ33360
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020623
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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