A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745209



Internal ID20521215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103008292..103008361hg38UCSC Ensembl
chr14:103474629..103474698hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281506
Samples
Known GenesCDC42BPB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745209
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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