A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515924



Internal ID20889285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:88572..220396hg38UCSC Ensembl
chr20:69213..201037hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38131825
hg19131825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202995
Samples
Known GenesDEFB125, DEFB126, DEFB127, DEFB128
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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