A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722720



Internal ID146386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30526443..30526743hg38UCSC Ensembl
chr19:31017350..31017650hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519412
Supporting Variants
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722720
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.054185


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