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nsv6885051

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,191

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 25 studies. See in: genome view    
    Submitted genomic97,734,581-97,737,771Question Mark
    Overlapping variant regions from other studies: 100 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):99,494,338-99,497,528Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6885051Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1097,734,58197,737,771
    nsv6885051RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1099,494,33899,497,528

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18341593deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18341593Submitted genomicNC_000010.11:g.977
    34581_97737771del
    GRCh38 (hg38)NC_000010.11Chr1097,734,58197,737,771
    nssv18341593RemappedPerfectNC_000010.10:g.994
    94338_99497528del
    GRCh37.p13First PassNC_000010.10Chr1099,494,33899,497,528

    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)
    nssv183415931.1e-053276148
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