A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533426



Internal ID309316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74864052..74865655hg38UCSC Ensembl
chr18:72576008..72577611hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg381604
hg191604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719513
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533426
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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