A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516775



Internal ID20890136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32609432..32620879hg38UCSC Ensembl
chr20:31197234..31208681hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3811448
hg1911448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516775
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