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nsv7047189

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,954

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 189 SVs from 40 studies. See in: genome view    
    Submitted genomic119,829,986-119,860,939Question Mark
    Overlapping variant regions from other studies: 191 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):120,372,609-120,403,562Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047189Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1119,829,986119,860,939
    nsv7047189RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1120,372,609120,403,562

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734624inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734624Submitted genomicNC_000001.11:g.119
    829986_119860939in
    v
    GRCh38 (hg38)NC_000001.11Chr1119,829,986119,860,939
    nssv18734624RemappedPerfectNC_000001.10:g.120
    372609_120403562in
    v
    GRCh37.p13First PassNC_000001.10Chr1120,372,609120,403,562

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18734624<0.00156273462
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