A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499989



Internal ID276940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38573287..38577203hg38UCSC Ensembl
chr13:39147424..39151340hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383917
hg193917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687001
Samples
Known GenesLINC00366
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer