A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498797



Internal ID275781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53531268..53539815hg38UCSC Ensembl
chr13:54105403..54113950hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg388548
hg198548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv132n206
Supporting Variantsnssv17687866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498797
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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