A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988659



Internal ID20555699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18584707..18600214hg38UCSC Ensembl
chr11:18606254..18621761hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3815508
hg1915508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449627
Supporting Variants
Samples
Known GenesSPTY2D1-AS1, UEVLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00117


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