U.S. flag

An official website of the United States government

nsv7077282

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,287

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 70 SVs from 17 studies. See in: genome view    
    Submitted genomic12,800,282-12,803,568Question Mark
    Overlapping variant regions from other studies: 70 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):12,703,599-12,706,885Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077282Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1712,800,28212,803,568
    nsv7077282RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1712,703,59912,706,885

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756110inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756110Submitted genomicNC_000017.11:g.128
    00282_12803568inv
    GRCh38 (hg38)NC_000017.11Chr1712,800,28212,803,568
    nssv18756110RemappedPerfectNC_000017.10:g.127
    03599_12706885inv
    GRCh37.p13First PassNC_000017.10Chr1712,703,59912,706,885

    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)
    nssv187561104e-061276268
    Support Center