A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094894



Internal ID20661934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135793671..135794611hg38UCSC Ensembl
chr3:135512513..135513453hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38941
hg19941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357856
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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