A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368525



Internal ID21026078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47359189..47368442hg38UCSC Ensembl
chr3:47400679..47409932hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg389254
hg199254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368525
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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