A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767377



Internal ID20543237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108741502..108741502hg38UCSC Ensembl
chr3:108460349..108460349hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767377
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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