A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986042



Internal ID20553082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103930399..103931061hg38UCSC Ensembl
chr11:103801127..103801789hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473331
Supporting Variants
Samples
Known GenesPDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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