A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041177



Internal ID20608217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:44462530..44463226hg38UCSC Ensembl
chr18:42042495..42043191hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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