A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852733



Internal ID22627668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133494415..133497609hg38UCSC Ensembl
chr8:134506658..134509852hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg383195
hg193195
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506899
Samples
Known GenesST3GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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