A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255069



Internal ID20822109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45121830..45123509hg38UCSC Ensembl
chr22:45517711..45519390hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381680
hg191680
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255069
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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