A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596432



Internal ID20969503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:455681..456826hg38UCSC Ensembl
chr20:436325..437470hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252128
Samples
Known GenesTBC1D20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596432
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