A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227177



Internal ID20794217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90347607..90348216hg38UCSC Ensembl
chr13:90999861..91000470hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227177
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00038


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