A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500838



Internal ID277761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60931545..60933002hg38UCSC Ensembl
chr13:61505679..61507136hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500838
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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