A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094848



Internal ID20661888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13489830..13491142hg38UCSC Ensembl
chr3:13531330..13532642hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357702
Supporting Variants
Samples
Known GenesHDAC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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