A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967899



Internal ID45920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58540380..58550867hg38UCSC Ensembl
chr5:57836207..57846694hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3810488
hg1910488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967899
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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