A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501935



Internal ID278818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58771927..58781754hg38UCSC Ensembl
chr13:59346061..59355888hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg389828
hg199828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501935
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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