A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362228



Internal ID21019781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24691884..24695651hg38UCSC Ensembl
chr3:24733375..24737142hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg383768
hg193768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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