A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722658



Internal ID146324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29520521..29520626hg38UCSC Ensembl
chr19:30011428..30011533hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530139
Supporting Variants
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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