A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664918



Internal ID21613225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34540657..34562467hg38UCSC Ensembl
chr14:35009863..35031673hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3821811
hg1921811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096871
Samples
Known GenesSNX6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664918
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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