A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969934



Internal ID22744869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24798102..24799477hg38UCSC Ensembl
chr22:25194069..25195444hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg381376
hg191376
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396332
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969934
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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