A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020211



Internal ID22081842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:138472272..138481268hg38UCSC Ensembl
Outerchr5:138469431..138482888hg38UCSC Ensembl
Innerchr5:137807961..137816957hg19UCSC Ensembl
Outerchr5:137805120..137818577hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3813458
hg1913458
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156386
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020211
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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