A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111128



Internal ID22020361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131317882..131647596hg38UCSC Ensembl
chr12:131802427..132132141hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38329715
hg19329715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609051
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111128
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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