A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369771



Internal ID21027324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146466701..146471700hg38UCSC Ensembl
chr3:146184488..146189487hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209704
Samples
Known GenesPLSCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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