A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868458



Internal ID22643394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89856000..89867711hg38UCSC Ensembl
chr15:90399232..90410943hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3811712
hg1911712
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474879, nssv17474880
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868458
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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