A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437927



Internal ID21095480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94879137..95091509hg38UCSC Ensembl
chr10:96638894..96851266hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38212373
hg19212373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984903
Samples
Known GenesCYP2C8, CYP2C9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437927
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