A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492501



Internal ID21150054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101734890..101735349hg38UCSC Ensembl
chr13:102387240..102387699hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006315
Samples
Known GenesFGF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492501
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