A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859458



Internal ID22634393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84885696..84899241hg38UCSC Ensembl
chr15:85428927..85442472hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3813546
hg1913546
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474308
Samples
Known GenesSLC28A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859458
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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