A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986242



Internal ID20553283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105970204..105971011hg38UCSC Ensembl
chr11:105840931..105841738hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472491
Supporting Variants
Samples
Known GenesGRIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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