A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755920



Internal ID20531780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23334144..23334144hg38UCSC Ensembl
chr20:23314781..23314781hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755920
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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