A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599483



Internal ID21548117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113617547..113617610hg38UCSC Ensembl
chr13:114271862..114271925hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094309
SamplesNA19238
Known GenesTFDP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599483
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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