A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360097



Internal ID21017650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141482501..141489900hg38UCSC Ensembl
chr3:141201343..141208742hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209642
Samples
Known GenesRASA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360097
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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