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nsv6604062

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,510

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 39 studies. See in: genome view    
    Submitted genomic99,603,627-99,608,136Question Mark
    Overlapping variant regions from other studies: 131 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):99,201,250-99,205,759Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6604062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,603,62799,608,136
    nsv6604062RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr799,201,25099,205,759

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18162439deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18162439Submitted genomicNC_000007.14:g.996
    03627_99608136del
    GRCh38 (hg38)NC_000007.14Chr799,603,62799,608,136
    nssv18162439RemappedPerfectNC_000007.13:g.992
    01250_99205759del
    GRCh37.p13First PassNC_000007.13Chr799,201,25099,205,759

    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)
    nssv18162439<0.001139254
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