A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389074



Internal ID21380209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93519919..93520285hg38UCSC Ensembl
chr9:96282201..96282567hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704696
Samples
Known GenesFAM120A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389074
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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