A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524924



Internal ID301106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36692140..36692937hg38UCSC Ensembl
chr18:34272103..34272900hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717380
Samples
Known GenesFHOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524924
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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