A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229846



Internal ID20796887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48199244..48206623hg38UCSC Ensembl
chr13:48773380..48780759hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg387380
hg197380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00684


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