A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575860



Internal ID20948931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80520404..80520961hg38UCSC Ensembl
chr14:80986748..80987305hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238195
Samples
Known GenesCEP128
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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