A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094376



Internal ID20661416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142923069..142924618hg38UCSC Ensembl
chr3:142641911..142643460hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381550
hg191550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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