A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857902



Internal ID22632837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4873290..4874689hg38UCSC Ensembl
chr9:4873290..4874689hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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