A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997693



Internal ID21907036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40591579..40591638hg38UCSC Ensembl
chr4:40593596..40593655hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545881
Samples
Known GenesRBM47
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997693
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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