A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762905



Internal ID20538765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40298239..40298239hg38UCSC Ensembl
chr20:38926879..38926879hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762905
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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