A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884721



Internal ID22659704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89860139..89861938hg38UCSC Ensembl
chr15:90403371..90405170hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474882, nssv17474883
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884721
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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