A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442839



Internal ID21100392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18507944..18525327hg38UCSC Ensembl
chr11:18529491..18546874hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3817384
hg1917384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988655
Samples
Known GenesTSG101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442839
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