A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759918



Internal ID20535778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86272069..86272069hg38UCSC Ensembl
chr11:85983111..85983111hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265715
Samples
Known GenesEED
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759918
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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