A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581337



Internal ID20954408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26844740..26846250hg38UCSC Ensembl
chr13:27418877..27420387hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381511
hg191511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581337
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