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nsv7052860

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:333,733

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1212 SVs from 78 studies. See in: genome view    
    Submitted genomic10,170,489-10,504,221Question Mark
    Overlapping variant regions from other studies: 1212 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):10,170,601-10,504,333Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr510,170,48910,504,221
    nsv7052860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr510,170,60110,504,333

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774613inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774613Submitted genomicNC_000005.10:g.101
    70489_10504221inv
    GRCh38 (hg38)NC_000005.10Chr510,170,48910,504,221
    nssv18774613RemappedPerfectNC_000005.9:g.1017
    0601_10504333inv
    GRCh37.p13First PassNC_000005.9Chr510,170,60110,504,333

    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)
    nssv187746134e-061276268
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