A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528189



Internal ID304257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76230289..76262830hg38UCSC Ensembl
chr18:73942244..73974785hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3832542
hg1932542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528189
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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