A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520454



Internal ID20893815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1378601..1383700hg38UCSC Ensembl
chr20:1359245..1364344hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065842
Samples
Known GenesFKBP1A, FKBP1A-SDCBP2, SDCBP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520454
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