A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929780



Internal ID22705039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39775560..39802294hg38UCSC Ensembl
chr18:37355524..37382258hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3826735
hg1926735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929780
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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