A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590188



Internal ID20963259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49681571..49682099hg38UCSC Ensembl
chr14:50148289..50148817hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226889
Samples
Known GenesPOLE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590188
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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