A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124533



Internal ID21406862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10873402..10873402hg38UCSC Ensembl
chr3:10915087..10915087hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38860
hg19860
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618591
Supporting Variants
SamplesHG00512
Known GenesSLC6A11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124533
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