A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995410



Internal ID20562450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92613562..92618101hg38UCSC Ensembl
chr11:92346728..92351267hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384540
hg194540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467982
Supporting Variants
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995410
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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