A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221103



Internal ID20788143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103571985..103572894hg38UCSC Ensembl
chr14:104038322..104039231hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593676
Supporting Variants
Samples
Known GenesAPOPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221103
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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