A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505024



Internal ID281813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68654730..68654828hg38UCSC Ensembl
chr13:69228862..69228960hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505024
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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