A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498667



Internal ID275654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114198455..114248967hg38UCSC Ensembl
chr13:114963930..115014442hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3850513
hg1950513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695665
Samples
Known GenesCDC16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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