A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098778



Internal ID20665818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178035799..178039414hg38UCSC Ensembl
chr3:177753587..177757202hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00115


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