A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519182



Internal ID295538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26943375..26954911hg38UCSC Ensembl
chr18:24523339..24534875hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3811537
hg1911537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716823
Samples
Known GenesCHST9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519182
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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