A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020630



Internal ID22082261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10318343..10319479hg38UCSC Ensembl
Outerchr5:10314452..10320334hg38UCSC Ensembl
Innerchr5:10318455..10319591hg19UCSC Ensembl
Outerchr5:10314564..10320446hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg385883
hg195883
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156311
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020630
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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