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nsv7017345

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,480

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 167 SVs from 35 studies. See in: genome view    
    Submitted genomic36,654,235-36,658,714Question Mark
    Overlapping variant regions from other studies: 167 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):37,145,137-37,149,616Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017345Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,654,23536,658,714
    nsv7017345RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,145,13737,149,616

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423288deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423288Submitted genomicNC_000019.10:g.366
    54235_36658714del
    GRCh38 (hg38)NC_000019.10Chr1936,654,23536,658,714
    nssv18423288RemappedPerfectNC_000019.9:g.3714
    5137_37149616del
    GRCh37.p13First PassNC_000019.9Chr1937,145,13737,149,616

    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)
    nssv184232884e-061276134
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