A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628694



Internal ID21576999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113654198..113654198hg38UCSC Ensembl
chr10:115413957..115413957hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068346
SamplesNA19239
Known GenesNRAP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628694
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