A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164684



Internal ID20731724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133502756..133503645hg38UCSC Ensembl
chr8:134514999..134515888hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433985
Supporting Variants
Samples
Known GenesST3GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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