A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722284



Internal ID145950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20948582..21383045hg38UCSC Ensembl
chr19:21131388..21565847hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540404
Supporting Variants
Samples
Known GenesZNF430, ZNF431, ZNF708, ZNF714, ZNF738, ZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722284
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.28551


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