A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589883



Internal ID20962954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103572112..103573200hg38UCSC Ensembl
chr14:104038449..104039537hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381089
hg191089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2250n223
Supporting Variantsnssv18235640
Samples
Known GenesAPOPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589883
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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