A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390173



Internal ID22211115
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3545222
Supporting Variants
SamplesHG00732
Known GenesRPS6KA5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390173
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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