A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582515



Internal ID21531029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165974126..165974436hg38UCSC Ensembl
chr4:166895278..166895588hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131948
SamplesNA19238
Known GenesTLL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582515
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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