A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720325



Internal ID143991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1967786..1968091hg38UCSC Ensembl
chr19:1967785..1968090hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514128
Supporting Variants
Samples
Known GenesCSNK1G2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720325
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.275765


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