A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765981



Internal ID20541841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14809242..14809242hg38UCSC Ensembl
chr3:14850749..14850749hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765981
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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