A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624867



Internal ID21573172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133959980..133959980hg38UCSC Ensembl
chr8:134972223..134972223hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg381055
hg191055
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141667
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624867
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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