A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079123



Internal ID21988356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121365532..121365532hg38UCSC Ensembl
chr4:122286687..122286687hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551455
Samples
Known GenesQRFPR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079123
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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