A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625667



Internal ID21817714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19953990..20144857hg38UCSC Ensembl
chr19:20064799..20255666hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38190868
hg19190868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054807
Supporting Variants
Samples
Known GenesZNF682, ZNF90
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625667
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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