A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041655



Internal ID20608695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34667691..34686346hg38UCSC Ensembl
chr18:32247655..32266310hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3818656
hg1918656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519007
Supporting Variants
Samples
Known GenesDTNA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer