A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473285



Internal ID21130838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112556023..112556651hg38UCSC Ensembl
chr11:112426746..112427374hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473285
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