A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555478



Internal ID328634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125797184..125805130hg38UCSC Ensembl
chr8:126809428..126817374hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg387947
hg197947
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17016350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555478
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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