A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581281



Internal ID20954352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45122795..45123140hg38UCSC Ensembl
chr14:45591998..45592343hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235787
Samples
Known GenesFKBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581281
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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