A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991637



Internal ID20558677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3828601..3830000hg38UCSC Ensembl
chr11:3849831..3851230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445561
Supporting Variants
Samples
Known GenesRHOG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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