A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469651



Internal ID21127204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44470773..44476211hg38UCSC Ensembl
chr11:44492323..44497761hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385439
hg195439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469651
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