A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639190



Internal ID21587495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143342646..143342646hg38UCSC Ensembl
chr8:144424816..144424816hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145392
SamplesHG03125
Known GenesTOP1MT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639190
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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