A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121120



Internal ID20688160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80094338..80095043hg38UCSC Ensembl
chr4:81015492..81016197hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390001
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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