A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453405



Internal ID22217842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14769189..15377775hg38UCSC Ensembl
chr16:14863046..15471632hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38608587
hg19608587
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3552103
Supporting Variants
SamplesHG00733
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR3180-4, MIR6511A-2, MIR6511B-1, MIR6770-2, NOMO1, NPIPA1, NPIPA5, NTAN1, PDXDC1, RRN3
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14453405
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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