A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233579



Internal ID20800619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77493830..77495559hg38UCSC Ensembl
chr13:78067965..78069694hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg381730
hg191730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer