A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735479



Internal ID20511421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104872109..104872244hg38UCSC Ensembl
chr14:105338446..105338581hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274094
Samples
Known GenesCEP170B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735479
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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