A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366040



Internal ID21023593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146160201..146162000hg38UCSC Ensembl
chr3:145877988..145879787hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209699
Samples
Known GenesPLOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366040
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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