A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16963131



Internal ID42749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20302977..20303059hg38UCSC Ensembl
chr5:20303086..20303168hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16963131
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002029


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