A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659017



Internal ID21607322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78755628..78755628hg38UCSC Ensembl
chr11:78466673..78466673hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076783
SamplesHG03371
Known GenesTENM4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659017
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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