A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044034



Internal ID20611075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75443669..75444081hg38UCSC Ensembl
chr18:73155624..73156036hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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