A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750569



Internal ID20526525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70126835..70126835hg38UCSC Ensembl
chr11:69972941..69972941hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286888
Samples
Known GenesANO1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750569
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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