A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027419



Internal ID21936762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38718683..38718949hg38UCSC Ensembl
chr18:36298647..36298913hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027419
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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