A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662240



Internal ID21610545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118705467..118705467hg38UCSC Ensembl
chr11:118576176..118576176hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072197
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662240
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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