A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529918



Internal ID305918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21782475..21783888hg38UCSC Ensembl
chr18:19362436..19363849hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381414
hg191414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716559
Samples
Known GenesMIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529918
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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