A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629683



Internal ID21821730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20413004..20535172hg38UCSC Ensembl
chr19:20595810..20717978hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38122169
hg19122169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041132
Supporting Variants
Samples
Known GenesZNF826P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629683
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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