A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722817



Internal ID146483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32434189..32434397hg38UCSC Ensembl
chr19:32925095..32925303hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525971
Supporting Variants
Samples
Known GenesDPY19L3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722817
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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