A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366196



Internal ID21023749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154550251..154559621hg38UCSC Ensembl
chr3:154268040..154277410hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg389371
hg199371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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