A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110820



Internal ID22020053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46227285..46227285hg38UCSC Ensembl
chr18:43807251..43807251hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg382569
hg192569
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622738
Samples
Known GenesC18orf25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110820
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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