A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264721



Internal ID20473939
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 StatusS
Merged Variantsnsv4733542
Supporting Variants
Samples
Known GenesFKBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264721
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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