A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv132n206



Internal ID22755436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53531268..53541778hg38UCSC Ensembl
chr13:54105403..54115913hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3810511
hg1910511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5503055, nsv5498797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv132n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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