A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433545



Internal ID212257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25204568..25204619hg38UCSC Ensembl
chr18:22784532..22784583hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716731
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433545
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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