A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062551



Internal ID20629591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66382167..66383515hg38UCSC Ensembl
chr1:66847850..66849198hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381349
hg191349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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