A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139098



Internal ID21497131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151256047..151256047hg38UCSC Ensembl
chr4:152177199..152177199hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617200
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139098
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