A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986828



Internal ID20553868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112980154..112994834hg38UCSC Ensembl
chr11:112850876..112865556hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3814681
hg1914681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469557
Supporting Variants
Samples
Known GenesNCAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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