A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097625



Internal ID20664665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184709003..184719614hg38UCSC Ensembl
chr3:184426791..184437402hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3810612
hg1910612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372393
Supporting Variants
Samples
Known GenesMAGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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