A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094808



Internal ID20661848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133956221..133957341hg38UCSC Ensembl
chr3:133675065..133676185hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366743
Supporting Variants
Samples
Known GenesSLCO2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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