A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693809



Internal ID117475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113260147..113260222hg38UCSC Ensembl
chr13:113914461..113914536hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497376
Supporting Variants
Samples
Known GenesCUL4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693809
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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