A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108585



Internal ID22017818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3295806..3295806hg38UCSC Ensembl
chr18:3295804..3295804hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382528
hg192528
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108585
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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