A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688081



Internal ID111747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57154300..57316106hg38UCSC Ensembl
chr13:57728434..57890240hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38161807
hg19161807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504736
Supporting Variants
Samples
Known GenesPRR20A, PRR20B, PRR20C, PRR20D, PRR20E
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688081
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001566


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