A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723152



Internal ID146818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37100938..37100989hg38UCSC Ensembl
chr19:37591840..37591891hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425432
Supporting Variants
Samples
Known GenesZNF420
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723152
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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