A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060119



Internal ID20627159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39621882..39622347hg38UCSC Ensembl
chr1:40087554..40088019hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00089


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