A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067683



Internal ID20634724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5096451..5097933hg38UCSC Ensembl
chr20:5077097..5078579hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381483
hg191483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522292
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer