A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366515



Internal ID21024068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4209110..4340569hg38UCSC Ensembl
chr3:4250794..4382253hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38131460
hg19131460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099884
Samples
Known GenesSETMAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366515
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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