A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733542



Internal ID20509472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45126249..45128097hg38UCSC Ensembl
chr14:45595452..45597300hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381849
hg191849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264721
Samples
Known GenesFKBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733542
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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