A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665078



Internal ID21613383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46896515..46916181hg38UCSC Ensembl
chr12:47290298..47309964hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3819667
hg1919667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088803
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665078
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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