A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723294



Internal ID146960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38925137..38929107hg38UCSC Ensembl
chr19:39415777..39419747hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383971
hg193971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533841
Supporting Variants
Samples
Known GenesSARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723294
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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