A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665969



Internal ID21614274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131293707..131663453hg38UCSC Ensembl
chr12:131778252..132147998hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38369747
hg19369747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077995
Samples
Known GenesLOC338797
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665969
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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