A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518072



Internal ID20891433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37911769..37913387hg38UCSC Ensembl
chr20:36540171..36541789hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381619
hg191619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068806
Samples
Known GenesVSTM2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518072
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