U.S. flag

An official website of the United States government

nsv6993218

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,930

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 20 studies. See in: genome view    
    Submitted genomic32,603,848-32,606,777Question Mark
    Overlapping variant regions from other studies: 95 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):30,930,866-30,933,795Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993218Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1732,603,84832,606,777
    nsv6993218RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1730,930,86630,933,795

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18407889deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18407889Submitted genomicNC_000017.11:g.326
    03848_32606777del
    GRCh38 (hg38)NC_000017.11Chr1732,603,84832,606,777
    nssv18407889RemappedPerfectNC_000017.10:g.309
    30866_30933795del
    GRCh37.p13First PassNC_000017.10Chr1730,930,86630,933,795

    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)
    nssv184078894e-061276116
    Support Center