A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628526



Internal ID21820573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22652221..22652387hg38UCSC Ensembl
chr19:22835023..22835189hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051724
Supporting Variants
Samples
Known GenesZNF492
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628526
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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