A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540284



Internal ID20913576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50423871..50436916hg38UCSC Ensembl
chr20:49040408..49053453hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3813046
hg1913046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540284
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