A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664343



Internal ID21612648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82841053..82841053hg38UCSC Ensembl
chr11:82552095..82552095hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076265
SamplesNA19238
Known GenesPRCP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664343
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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