A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940982



Internal ID22716398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38564292..38564585hg38UCSC Ensembl
chr18:36144256..36144549hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940982
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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