A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610195



Internal ID21802242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45119420..45119706hg38UCSC Ensembl
chr14:45588623..45588909hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026267
Supporting Variants
Samples
Known GenesFKBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610195
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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