A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370290



Internal ID22261234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63545833..63566393hg38UCSC Ensembl
chr14:64012551..64033111hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3820561
hg1920561
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3237686
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370290
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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