A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370217



Internal ID22276240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60447092..60474520hg38UCSC Ensembl
chr14:60913810..60941238hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3827429
hg1927429
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236804
Supporting Variants
SamplesNA19239
Known GenesC14orf39
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370217
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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