A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109878



Internal ID22019111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21378873..21562827hg38UCSC Ensembl
chr22:21733162..21917116hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38183955
hg19183955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645516
Samples
Known GenesHIC2, PI4KAP2, RIMBP3B, RIMBP3C, TMEM191C, UBE2L3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109878
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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