A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516108



Internal ID20889469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12373082..12373789hg38UCSC Ensembl
chr18:12373081..12373788hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039395
Samples
Known GenesAFG3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516108
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