A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072189



Internal ID21475640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114356849..114356849hg38UCSC Ensembl
chr11:114227571..114227571hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647055
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072189
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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