A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985286



Internal ID20552326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94670157..94794660hg38UCSC Ensembl
chr10:96429914..96554417hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38124504
hg19124504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452430
Supporting Variants
Samples
Known GenesCYP2C18, CYP2C19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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