A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504736



Internal ID281531
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 StatusM
Merged Variants
Supporting Variantsnssv17688081
Samples
Known GenesPRR20A, PRR20B, PRR20C, PRR20D, PRR20E
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504736
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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