A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093050



Internal ID20660090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105157895..105234956hg38UCSC Ensembl
chr3:104876739..104953800hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3877062
hg1977062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375353
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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