A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110392



Internal ID22019625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25033665..25033665hg38UCSC Ensembl
chr18:22613629..22613629hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110392
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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