A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3545222



Internal ID22414239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91051958..91052212hg38UCSC Ensembl
chr14:91518302..91518556hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390173
SamplesHG00732
Known GenesRPS6KA5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3545222
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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