A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597316



Internal ID20970387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33467208..33467967hg38UCSC Ensembl
chr20:32055014..32055773hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597316
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