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nsv6387040

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:466

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 27 studies. See in: genome view    
    Submitted genomic65,688,087-65,688,552Question Mark
    Overlapping variant regions from other studies: 126 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):66,553,805-66,554,270Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6387040Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr465,688,08765,688,552
    nsv6387040RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr466,553,80566,554,270

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18118327deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18118327Submitted genomicNC_000004.12:g.656
    88087_65688552del
    GRCh38 (hg38)NC_000004.12Chr465,688,08765,688,552
    nssv18118327RemappedPerfectNC_000004.11:g.665
    53805_66554270del
    GRCh37.p13First PassNC_000004.11Chr466,553,80566,554,270

    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)
    nssv18118327<0.001837446
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