A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722283



Internal ID145949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20944502..20944581hg38UCSC Ensembl
chr19:21127308..21127387hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526143
Supporting Variants
Samples
Known GenesZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722283
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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