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nsv6897074

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,213

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
    Submitted genomic91,339,058-91,346,270Question Mark
    Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):93,098,815-93,106,027Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6897074Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1091,339,05891,346,270
    nsv6897074RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1093,098,81593,106,027

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18341036deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18341036Submitted genomicNC_000010.11:g.913
    39058_91346270del
    GRCh38 (hg38)NC_000010.11Chr1091,339,05891,346,270
    nssv18341036RemappedPerfectNC_000010.10:g.930
    98815_93106027del
    GRCh37.p13First PassNC_000010.10Chr1093,098,81593,106,027

    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)
    nssv183410361.4e-054276180
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