A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866478



Internal ID22641413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58140906..58151850hg38UCSC Ensembl
chr15:58433105..58444049hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3810945
hg1910945
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472937
Samples
Known GenesAQP9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866478
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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