A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754066



Internal ID20529926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219159501..219159501hg38UCSC Ensembl
chr2:220024223..220024223hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292590
Samples
Known GenesNHEJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754066
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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