A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595708



Internal ID20968779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17694612..17695407hg38UCSC Ensembl
chr20:17675257..17676052hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253591
Samples
Known GenesBANF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595708
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