A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099884



Internal ID20666924
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 StatusS
Merged Variantsnsv6366515
Supporting Variants
Samples
Known GenesSETMAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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