A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062550



Internal ID20629590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66367582..66368112hg38UCSC Ensembl
chr1:66833265..66833795hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334108
Supporting Variants
Samples
Known GenesPDE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062550
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