A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597888



Internal ID20970959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35781115..35781677hg38UCSC Ensembl
chr20:34369037..34369599hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252517
Samples
Known GenesPHF20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597888
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