A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667987



Internal ID21616294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:310101..320160hg38UCSC Ensembl
chr11:310101..320160hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3810060
hg1910060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074560
Samples
Known GenesIFITM1, IFITM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667987
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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