A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582857



Internal ID20955928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80453738..80459402hg38UCSC Ensembl
chr13:81027873..81033537hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg385665
hg195665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582857
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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