A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273043



Internal ID20482261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34817117..34817196hg38UCSC Ensembl
chr20:33404920..33404999hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731986
Supporting Variants
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273043
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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