A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997685



Internal ID21907028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40136394..40168739hg38UCSC Ensembl
chr4:40138014..40170359hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3832346
hg1932346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541700
Samples
Known GenesN4BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997685
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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