A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511394



Internal ID287977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89553408..89850362hg38UCSC Ensembl
chr13:90205662..90502616hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38296955
hg19296955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691137
Samples
Known GenesLINC00353
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511394
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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