A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526350



Internal ID302483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76895884..76895941hg38UCSC Ensembl
chr18:74607840..74607897hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719656
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526350
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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