A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293148



Internal ID20502366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20081272..20081272hg38UCSC Ensembl
chr20:20061916..20061916hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382697
hg192697
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754832
Supporting Variants
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293148
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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