A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992707



Internal ID20559747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69487321..69530633hg38UCSC Ensembl
chr11:69302089..69345401hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3843313
hg1943313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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