A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989861



Internal ID20556901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28092571..28290347hg38UCSC Ensembl
chr11:28114118..28311894hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38197777
hg19197777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450622
Supporting Variants
Samples
Known GenesKIF18A, METTL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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