A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986862



Internal ID20553902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113349659..113351497hg38UCSC Ensembl
chr11:113220381..113222219hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg381839
hg191839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462376
Supporting Variants
Samples
Known GenesTTC12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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