A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555789



Internal ID328939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78178142..78203273hg38UCSC Ensembl
chr18:75938142..75963273hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3825132
hg1925132
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555789
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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