A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725211



Internal ID148877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43951851..43952172hg38UCSC Ensembl
chr19:44456003..44456324hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525244
Supporting Variants
Samples
Known GenesZNF221
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725211
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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