A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220918



Internal ID20787958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95240812..95244159hg38UCSC Ensembl
chr13:95893066..95896413hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg383348
hg193348
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579864
Supporting Variants
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220918
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00033


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