A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530895



Internal ID20904256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22813472..22818005hg38UCSC Ensembl
chr18:20393435..20397968hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384534
hg194534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530895
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