A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918920



Internal ID22694142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99828561..99828680hg38UCSC Ensembl
chr9:102590843..102590962hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448536
Samples
Known GenesNR4A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918920
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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