A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059559



Internal ID20626599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243424618..243425402hg38UCSC Ensembl
chr1:243587920..243588704hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324862
Supporting Variants
Samples
Known GenesSDCCAG8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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