A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563678



Internal ID336608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85344110..85344328hg38UCSC Ensembl
chr8:86256339..86256557hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015470
Samples
Known GenesCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563678
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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