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nsv7077305

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,409

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 20 studies. See in: genome view    
    Submitted genomic87,999,274-88,001,682Question Mark
    Overlapping variant regions from other studies: 116 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):88,542,505-88,544,913Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077305Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1587,999,27488,001,682
    nsv7077305RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1588,542,50588,544,913

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756080inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756080Submitted genomicNC_000015.10:g.879
    99274_88001682inv
    GRCh38 (hg38)NC_000015.10Chr1587,999,27488,001,682
    nssv18756080RemappedPerfectNC_000015.9:g.8854
    2505_88544913inv
    GRCh37.p13First PassNC_000015.9Chr1588,542,50588,544,913

    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)
    nssv187560804e-061276268
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