A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722383



Internal ID146049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21859999..22962000hg38UCSC Ensembl
chr19:22042801..23144802hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381102002
hg191102002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526651
Supporting Variants
Samples
Known GenesLOC100996349, LOC440518, ZNF208, ZNF257, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722383
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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