A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498169



Internal ID275171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33734878..33735279hg38UCSC Ensembl
chr13:34309015..34309416hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498169
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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