A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986781



Internal ID20553821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111928660..111936507hg38UCSC Ensembl
chr11:111799384..111807231hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg387848
hg197848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470062
Supporting Variants
Samples
Known GenesDIXDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986781
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