A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987113



Internal ID20554155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116797701..116801700hg38UCSC Ensembl
chr11:116668417..116672416hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01146


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