A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075733



Internal ID21488602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62426177..62426177hg38UCSC Ensembl
chr11:62193649..62193649hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662795
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075733
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