A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137141



Internal ID20704181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116286584..116287386hg38UCSC Ensembl
chr6:116607747..116608549hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610694
Supporting Variants
Samples
Known GenesDSE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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