A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766710



Internal ID20542570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141431323..141431323hg38UCSC Ensembl
chr3:141150165..141150165hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282502
Samples
Known GenesZBTB38
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766710
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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