A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585232



Internal ID21533778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89723438..89723569hg38UCSC Ensembl
chr12:90117215..90117346hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079720
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585232
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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