A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400185



Internal ID22458055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11318838..11561925hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38243088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967892
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400185
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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