A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721758



Internal ID145424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15309000..15316000hg38UCSC Ensembl
chr19:15419811..15426811hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg387001
hg197001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721758
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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