A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867550



Internal ID22642485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86979309..86982110hg38UCSC Ensembl
chr15:87522540..87525341hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474328, nssv17474327
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867550
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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