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nsv6488448

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:996,910

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1978 SVs from 68 studies. See in: genome view    
    Submitted genomic96,013,973-97,010,882Question Mark
    Overlapping variant regions from other studies: 1978 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):96,666,227-97,663,136Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6488448Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1396,013,97397,010,882
    nsv6488448RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1396,666,22797,663,136

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18015574deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18015574Submitted genomicNC_000013.11:g.960
    13973_97010882del
    GRCh38 (hg38)NC_000013.11Chr1396,013,97397,010,882
    nssv18015574RemappedPerfectNC_000013.10:g.966
    66227_97663136del
    GRCh37.p13First PassNC_000013.10Chr1396,666,22797,663,136

    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)
    nssv18015574<0.001139182
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