A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518679



Internal ID20892040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11666781..11668022hg38UCSC Ensembl
chr20:11647429..11648670hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518679
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