A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050716



Internal ID21959949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28220479..28220479hg38UCSC Ensembl
chr3:28261970..28261970hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050716
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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