A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093926



Internal ID20660966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139106403..139107180hg38UCSC Ensembl
chr3:138825245..138826022hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360795
Supporting Variants
Samples
Known GenesBPESC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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