A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524444



Internal ID20897805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19162627..19188123hg38UCSC Ensembl
chr20:19143271..19168767hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3825497
hg1925497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524444
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