A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759529



Internal ID20535389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21046044..21046044hg38UCSC Ensembl
chr20:21026685..21026685hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759529
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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