A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927087



Internal ID22702315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97076668..97083615hg38UCSC Ensembl
chr9:99838950..99845897hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386948
hg196948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448006
Samples
Known GenesLOC340508
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927087
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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