A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909472



Internal ID22684682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99862498..99862580hg38UCSC Ensembl
chr9:102624780..102624862hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442419
Samples
Known GenesNR4A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909472
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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