A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993215



Internal ID20560255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62578446..62585970hg38UCSC Ensembl
chr11:62345918..62353442hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg387525
hg197525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466204
Supporting Variants
Samples
Known GenesTUT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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