A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936050



Internal ID24747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73561566..73564524hg38UCSC Ensembl
chr3:73610717..73613675hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382959
hg192959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437332
Supporting Variants
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936050
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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