A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563821



Internal ID336748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94829509..94861959hg38UCSC Ensembl
chr12:95223285..95255735hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3832451
hg1932451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684199
Samples
Known GenesKRT19P2, MIR492
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563821
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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