A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667425



Internal ID21615730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21424744..21510142hg38UCSC Ensembl
chr22:21779033..21864431hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3885399
hg1985399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135111
Samples
Known GenesHIC2, PI4KAP2, TMEM191C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667425
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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