A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134310



Internal ID21450692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18158935..18158935hg38UCSC Ensembl
chr3:18200427..18200427hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616332
Supporting Variants
SamplesHG01505
Known GenesLOC339862
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134310
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