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nsv7017910

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,355

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 216 SVs from 21 studies. See in: genome view    
    Submitted genomic9,596,751-9,599,105Question Mark
    Overlapping variant regions from other studies: 216 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):9,596,749-9,599,103Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017910Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr189,596,7519,599,105
    nsv7017910RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr189,596,7499,599,103

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18420715deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18420715Submitted genomicNC_000018.10:g.959
    6751_9599105del
    GRCh38 (hg38)NC_000018.10Chr189,596,7519,599,105
    nssv18420715RemappedPerfectNC_000018.9:g.9596
    749_9599103del
    GRCh37.p13First PassNC_000018.9Chr189,596,7499,599,103

    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)
    nssv184207157e-062275826
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