A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763121



Internal ID20538981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40240765..40240765hg38UCSC Ensembl
chr20:38869405..38869405hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763121
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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