A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762830



Internal ID20538690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94460356..94460356hg38UCSC Ensembl
chr3:94179200..94179200hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762830
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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