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nsv7008007

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,933

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 31 studies. See in: genome view    
    Submitted genomic4,481,615-4,487,547Question Mark
    Overlapping variant regions from other studies: 143 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):4,481,612-4,487,544Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7008007Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr194,481,6154,487,547
    nsv7008007RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr194,481,6124,487,544

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423882deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423882Submitted genomicNC_000019.10:g.448
    1615_4487547del
    GRCh38 (hg38)NC_000019.10Chr194,481,6154,487,547
    nssv18423882RemappedPerfectNC_000019.9:g.4481
    612_4487544del
    GRCh37.p13First PassNC_000019.9Chr194,481,6124,487,544

    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)
    nssv184238821.4e-054275928
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