A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852908



Internal ID22627843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45126109..45128108hg38UCSC Ensembl
chr14:45595312..45597311hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455067
Samples
Known GenesFKBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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