A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131478



Internal ID21486450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57578465..57578465hg38UCSC Ensembl
chr3:57564192..57564192hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606547
Supporting Variants
SamplesNA12878
Known GenesARF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131478
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