A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094106



Internal ID21414885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58484719..58484719hg38UCSC Ensembl
chr15:58776918..58776918hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647564
Supporting Variants
SamplesHG00513
Known GenesLIPC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094106
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