A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851859



Internal ID22626794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58136839..58139988hg38UCSC Ensembl
chr15:58429038..58432187hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472936
Samples
Known GenesAQP9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851859
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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