A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642384



Internal ID21590689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88155365..88155365hg38UCSC Ensembl
chr10:89915122..89915122hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072002
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642384
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