A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539789



Internal ID20913084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45493319..45494120hg38UCSC Ensembl
chr20:44121959..44122760hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539789
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