A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662097



Internal ID21610402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100829390..100829390hg38UCSC Ensembl
chr11:100700121..100700121hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072654
SamplesHG03683
Known GenesARHGAP42
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662097
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