A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111504



Internal ID22020737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131038127..131577491hg38UCSC Ensembl
chr12:131522672..132062036hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38539365
hg19539365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617384
Samples
Known GenesGPR133, LOC116437, LOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111504
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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