A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866013



Internal ID22640948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84912692..84916794hg38UCSC Ensembl
chr15:85455923..85460025hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg384103
hg194103
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474311
Samples
Known GenesSLC28A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866013
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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