A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584761



Internal ID21533305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28051794..28052343hg38UCSC Ensembl
chr13:28625931..28626480hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094401
SamplesNA12878
Known GenesFLT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584761
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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