A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910588



Internal ID22685799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93451376..93451448hg38UCSC Ensembl
chr9:96213658..96213730hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436808
Samples
Known GenesFAM120AOS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910588
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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