A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993644



Internal ID20560684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75329468..75330482hg38UCSC Ensembl
chr11:75040512..75041526hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468533
Supporting Variants
Samples
Known GenesARRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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