A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962839



Internal ID42548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16272106..16276946hg38UCSC Ensembl
chr5:16272215..16277055hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg384841
hg194841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962839
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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