A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645244



Internal ID21593549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75392544..75392544hg38UCSC Ensembl
chr15:75684885..75684885hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088532
SamplesHG00733
Known GenesSIN3A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645244
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