A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108588



Internal ID22017821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46636683..46639525hg38UCSC Ensembl
chr12:47030466..47033308hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg382843
hg192843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108588
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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