A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281856



Internal ID20491074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78464564..78464717hg38UCSC Ensembl
chr11:78175610..78175763hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745759
Supporting Variants
Samples
Known GenesNARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281856
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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