A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756007



Internal ID20531867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110452058..110452058hg38UCSC Ensembl
chr11:110322782..110322782hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259370
Samples
Known GenesFDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756007
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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