A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463888



Internal ID21121441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124539858..124705383hg38UCSC Ensembl
chr11:124409754..124575279hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38165526
hg19165526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987828
Samples
Known GenesOR8A1, OR8B12, PANX3, SIAE, SPA17, TBRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463888
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