A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996461



Internal ID20563501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93268001..93277400hg38UCSC Ensembl
chr11:93001167..93010566hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996461
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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