A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280050



Internal ID20489268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14130072..14130424hg38UCSC Ensembl
chr11:14151618..14151970hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735668
Supporting Variants
Samples
Known GenesSPON1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280050
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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