A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459327



Internal ID22269397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60604530..60613253hg38UCSC Ensembl
chr14:61071248..61079971hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388724
hg198724
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3246766
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459327
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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