A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722828



Internal ID146494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32601150..32614480hg38UCSC Ensembl
chr19:33092056..33105386hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3813331
hg1913331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515023
Supporting Variants
Samples
Known GenesANKRD27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722828
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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