A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231509



Internal ID20798549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85178455..85181024hg38UCSC Ensembl
chr13:85752590..85755159hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg382570
hg192570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231509
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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