A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020619



Internal ID22082250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3143394..3163574hg38UCSC Ensembl
Outerchr5:3143095..3165044hg38UCSC Ensembl
Innerchr5:3143508..3163688hg19UCSC Ensembl
Outerchr5:3143209..3165158hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3821950
hg1921950
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156302
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020619
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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