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nsv7045257

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,073

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 25 studies. See in: genome view    
    Submitted genomic87,166,839-87,170,911Question Mark
    Overlapping variant regions from other studies: 120 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):87,632,522-87,636,594Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045257Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr187,166,83987,170,911
    nsv7045257RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr187,632,52287,636,594

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763239inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763239Submitted genomicNC_000001.11:g.871
    66839_87170911inv
    GRCh38 (hg38)NC_000001.11Chr187,166,83987,170,911
    nssv18763239RemappedPerfectNC_000001.10:g.876
    32522_87636594inv
    GRCh37.p13First PassNC_000001.10Chr187,632,52287,636,594

    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)
    nssv187632397e-062274806
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