A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020620



Internal ID22082251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3953496..3973693hg38UCSC Ensembl
Outerchr5:3949095..3978788hg38UCSC Ensembl
Innerchr5:3953610..3973807hg19UCSC Ensembl
Outerchr5:3949209..3978902hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3829694
hg1929694
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156303
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020620
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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