A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704696



Internal ID21376972
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 StatusS
Merged Variantsnsv4389074
Supporting Variants
Samples
Known GenesFAM120A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704696
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.195402


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