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nsv7061946

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:383,493

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1584 SVs from 81 studies. See in: genome view    
    Submitted genomic45,393,770-45,777,262Question Mark
    Overlapping variant regions from other studies: 1584 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):45,897,028-46,280,520Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061946Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1945,393,77045,777,262
    nsv7061946RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1945,897,02846,280,520

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760796inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760796Submitted genomicNC_000019.10:g.453
    93770_45777262inv
    GRCh38 (hg38)NC_000019.10Chr1945,393,77045,777,262
    nssv18760796RemappedPerfectNC_000019.9:g.4589
    7028_46280520inv
    GRCh37.p13First PassNC_000019.9Chr1945,897,02846,280,520

    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)
    nssv187607964e-061276268
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