A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755417



Internal ID20531277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93744963..93744963hg38UCSC Ensembl
chr11:93478129..93478129hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290489
Samples
Known GenesC11orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755417
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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