A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597768



Internal ID20970839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41103316..41104119hg38UCSC Ensembl
chr20:39731956..39732759hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252034
Samples
Known GenesTOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597768
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