A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754832



Internal ID20530692
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 StatusM
Merged Variants
Supporting Variantsnssv16293148
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754832
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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