A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648817



Internal ID21597122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79438270..79438270hg38UCSC Ensembl
chr15:79730612..79730612hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095624
SamplesNA12878
Known GenesKIAA1024
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648817
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