A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967728



Internal ID45798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43429102..43429492hg38UCSC Ensembl
chr5:43429204..43429594hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967728
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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