A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404968



Internal ID22462838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69981404..69984180hg38UCSC Ensembl
chr18:67648640..67651416hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg382777
hg192777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933757
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404968
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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