A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281864



Internal ID20491082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108058027..108058120hg38UCSC Ensembl
chr11:107928754..107928847hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734899
Supporting Variants
Samples
Known GenesCUL5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281864
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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