A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557683



Internal ID330774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127339667..127339991hg38UCSC Ensembl
chr8:128351912..128352236hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17018092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557683
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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