A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850642



Internal ID22625577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35226489..35228521hg38UCSC Ensembl
chr9:35226486..35228518hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382033
hg192033
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513013
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850642
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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