A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879365



Internal ID22654334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93103168..93104467hg38UCSC Ensembl
chr15:93646397..93647696hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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