A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254971



Internal ID20822011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38597930..38599163hg38UCSC Ensembl
chr22:38993935..38995168hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598842
Supporting Variants
Samples
Known GenesFAM227A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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