A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583964



Internal ID21532496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143342539..143342610hg38UCSC Ensembl
chr8:144424709..144424780hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140936
SamplesNA19238
Known GenesTOP1MT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583964
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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