A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996066



Internal ID20563106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9908441..9912402hg38UCSC Ensembl
chr11:9929988..9933949hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383962
hg193962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450647
Supporting Variants
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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