A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993583



Internal ID20560623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68503233..68511268hg38UCSC Ensembl
chr11:68270701..68278736hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg388036
hg198036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456025
Supporting Variants
Samples
Known GenesPPP6R3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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