A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995083



Internal ID20562123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9868208..9937482hg38UCSC Ensembl
chr11:9889755..9959029hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3869275
hg1969275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436415
Supporting Variants
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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