A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094863



Internal ID20661903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13532298..13536684hg38UCSC Ensembl
chr3:13573798..13578184hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384387
hg194387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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