A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102946



Internal ID20669986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58532455..58539986hg38UCSC Ensembl
chr3:58518182..58525713hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg387532
hg197532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367165
Supporting Variants
Samples
Known GenesACOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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