A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070142



Internal ID21979375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189001595..189001595hg38UCSC Ensembl
chr3:188719384..188719384hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381356
hg191356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070142
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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