A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590857



Internal ID21539427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107904280..107904599hg38UCSC Ensembl
chr12:108298057..108298376hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077112
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590857
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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