A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589858



Internal ID21538425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108859886..108859955hg38UCSC Ensembl
chr12:109253662..109253731hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076761
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589858
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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