A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375493



Internal ID21033046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153017318..153042937hg38UCSC Ensembl
chr3:152735107..152760726hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3825620
hg1925620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375493
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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