A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563235



Internal ID336172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50026611..50026900hg38UCSC Ensembl
chr12:50420394..50420683hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17056443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563235
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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