A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723327



Internal ID146993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39241418..39244559hg38UCSC Ensembl
chr19:39732058..39735199hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528649
Supporting Variants
Samples
Known GenesIFNL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723327
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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