A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590026



Internal ID21538594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83049519..83055591hg38UCSC Ensembl
chr9:85664434..85670506hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg386073
hg196073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162705
SamplesHG03125
Known GenesRASEF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590026
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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