A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556529



Internal ID329666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75713792..75731143hg38UCSC Ensembl
chr12:76107572..76124923hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3817352
hg1917352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17689241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556529
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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