A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966351



Internal ID44886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32628352..32630604hg38UCSC Ensembl
chr5:32628458..32630710hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg382253
hg192253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966351
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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