A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620367



Internal ID21812414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53923028..53923242hg38UCSC Ensembl
chr19:54426282..54426496hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048486
Supporting Variants
Samples
Known GenesCACNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620367
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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