A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660789



Internal ID21609094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97026294..97026294hg38UCSC Ensembl
chr12:97420072..97420072hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098658
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660789
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