A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086813



Internal ID21452495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55303274..55303752hg38UCSC Ensembl
chr15:55595472..55595950hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585269
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086813
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer