A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545303



Internal ID20918533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62185367..62190768hg38UCSC Ensembl
chr20:60760423..60765824hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385402
hg195402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068326
Samples
Known GenesMTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer