A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597092



Internal ID21545703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85313486..85313535hg38UCSC Ensembl
chr9:87928401..87928450hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163089
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597092
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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