A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454516



Internal ID21112069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14477109..14478469hg38UCSC Ensembl
chr11:14498655..14500015hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988325
Samples
Known GenesCOPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454516
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