A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586061



Internal ID21534611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117075868..117075984hg38UCSC Ensembl
chr12:117513673..117513789hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077260
SamplesHG03486
Known GenesTESC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586061
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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