A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502058



Internal ID278936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70349280..70549429hg38UCSC Ensembl
chr13:70923412..71123561hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38200150
hg19200150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502058
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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