A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135337



Internal ID21502898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26671373..26671373hg38UCSC Ensembl
chr3:26712864..26712864hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612649
Supporting Variants
SamplesNA19239
Known GenesLRRC3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135337
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