A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717363



Internal ID141029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36373025..36375764hg38UCSC Ensembl
chr18:33952988..33955727hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528389
Supporting Variants
Samples
Known GenesFHOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717363
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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