A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159000



Internal ID21509415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89422249..89422249hg38UCSC Ensembl
chr5:88718066..88718066hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641298
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159000
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