A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253775



Internal ID20820815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40097362..40098384hg38UCSC Ensembl
chr22:40493366..40494388hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596614
Supporting Variants
Samples
Known GenesTNRC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253775
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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