A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083019



Internal ID21504779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61381877..61381877hg38UCSC Ensembl
chr15:61674076..61674076hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663892
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083019
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