A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518645



Internal ID295025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35794801..35813677hg38UCSC Ensembl
chr18:33374765..33393641hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3818877
hg1918877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518645
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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