A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362968



Internal ID21020521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141637680..141638657hg38UCSC Ensembl
chr3:141356522..141357499hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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