A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106481



Internal ID21448704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57379746..57379746hg38UCSC Ensembl
chr19:57891114..57891114hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649850
Supporting Variants
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106481
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