A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156322



Internal ID22084798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20554801..20564211hg38UCSC Ensembl
Outerchr5:20550381..20566972hg38UCSC Ensembl
Innerchr5:20554910..20564320hg19UCSC Ensembl
Outerchr5:20550490..20567081hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3816592
hg1916592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020742
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156322
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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