A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664845



Internal ID21613152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169358122..169388085hg38UCSC Ensembl
chr4:170279273..170309236hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3829964
hg1929964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130660
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664845
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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