A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038736



Internal ID21948079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24938770..24938822hg38UCSC Ensembl
chr18:22518734..22518786hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038736
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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