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nsv6836477

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,798

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 79 SVs from 20 studies. See in: genome view    
    Submitted genomic43,313,708-43,316,505Question Mark
    Overlapping variant regions from other studies: 79 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):43,353,307-43,356,104Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6836477Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr743,313,70843,316,505
    nsv6836477RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr743,353,30743,356,104

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18542339deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18542339Submitted genomicNC_000007.14:g.433
    13708_43316505del
    GRCh38 (hg38)NC_000007.14Chr743,313,70843,316,505
    nssv18542339RemappedPerfectNC_000007.13:g.433
    53307_43356104del
    GRCh37.p13First PassNC_000007.13Chr743,353,30743,356,104

    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)
    nssv185423394e-061275772
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