A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513052



Internal ID289585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76251351..76253129hg38UCSC Ensembl
chr13:76825487..76827265hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg381779
hg191779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513052
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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