A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102129



Internal ID22011363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57792125..57945458hg38UCSC Ensembl
chr14:58258843..58412176hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38153334
hg19153334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609747
Samples
Known GenesSLC35F4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102129
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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