A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723272



Internal ID146938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38730660..38733010hg38UCSC Ensembl
chr19:39221300..39223650hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382351
hg192351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516593
Supporting Variants
Samples
Known GenesCAPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723272
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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