A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103103



Internal ID21506728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9866433..9866433hg38UCSC Ensembl
chr18:9866430..9866430hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653015
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103103
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