A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637929



Internal ID21586234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107694754..107694754hg38UCSC Ensembl
chr8:108706982..108706982hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143115
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637929
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer