A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492012



Internal ID21149565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99848800..99849292hg38UCSC Ensembl
chr13:100501054..100501546hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016431
Samples
Known GenesCLYBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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