A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514779



Internal ID22572738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93444835..93449352hg38UCSC Ensembl
chr9:96207117..96211634hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384518
hg194518
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865586
Supporting Variants
Samples
Known GenesFAM120AOS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514779
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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