A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110395



Internal ID22019628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75121838..75121838hg38UCSC Ensembl
chr18:72833794..72833794hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110395
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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