A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534762



Internal ID310521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:43792523..43792527hg38UCSC Ensembl
chr18:41372488..41372492hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534762
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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