A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934123



Internal ID23481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74353651..74357990hg38UCSC Ensembl
chr3:74402802..74407141hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg384340
hg194340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446697
Supporting Variants
Samples
Known GenesCNTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.005151


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