A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467298



Internal ID21124851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40181560..40182144hg38UCSC Ensembl
chr11:40203110..40203694hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991065
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467298
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