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nsv6528594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,542

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 194 SVs from 24 studies. See in: genome view    
    Submitted genomic31,586,886-31,596,427Question Mark
    Overlapping variant regions from other studies: 194 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):29,166,849-29,176,390Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6528594Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1831,586,88631,596,427
    nsv6528594RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1829,166,84929,176,390

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18039929deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18039929Submitted genomicNC_000018.10:g.315
    86886_31596427del
    GRCh38 (hg38)NC_000018.10Chr1831,586,88631,596,427
    nssv18039929RemappedPerfectNC_000018.9:g.2916
    6849_29176390del
    GRCh37.p13First PassNC_000018.9Chr1829,166,84929,176,390

    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)
    nssv18039929<0.001139268
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