A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996201



Internal ID21905544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154807205..154807259hg38UCSC Ensembl
chr4:155728357..155728411hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556977
Samples
Known GenesRBM46
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996201
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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