A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646394



Internal ID21594699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70006402..70006402hg38UCSC Ensembl
chr11:69852508..69852508hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075819
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646394
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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