A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234935



Internal ID20801975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82300839..82301732hg38UCSC Ensembl
chr13:82874974..82875867hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577427
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234935
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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