A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855092



Internal ID22630027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129125813..129130190hg38UCSC Ensembl
chr9:131888092..131892469hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384378
hg194378
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511463
Samples
Known GenesPPP2R4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855092
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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