A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520155



Internal ID296492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26950615..26987183hg38UCSC Ensembl
chr18:24530579..24567147hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3836569
hg1936569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716824
Samples
Known GenesCHST9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520155
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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