A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672103



Internal ID21620408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21151085..21458186hg38UCSC Ensembl
chr22:21505374..21812475hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38307102
hg19307102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123192
SamplesHG00731
Known GenesFAM230B, HIC2, POM121L8P, RIMBP3B, RIMBP3C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672103
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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