A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561686



Internal ID334656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70570052..70570298hg38UCSC Ensembl
chr18:68237288..68237534hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561686
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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