A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755166



Internal ID20531026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2475214..2475214hg38UCSC Ensembl
chr20:2455860..2455860hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755166
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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