A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526775



Internal ID302891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12045735..12090600hg38UCSC Ensembl
chr18:12045734..12090599hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3844866
hg1944866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526775
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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