A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932873



Internal ID22708178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67371048..67931569hg38UCSC Ensembl
chr18:65038285..65598806hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38560522
hg19560522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389710
Samples
Known GenesDSEL, LOC643542
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932873
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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