A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17719334



Internal ID143000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71913791..72260374hg38UCSC Ensembl
chr18:69581027..69927609hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38346584
hg19346583
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17719334
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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