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nsv6829277

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,658

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 27 studies. See in: genome view    
    Submitted genomic77,400,769-77,408,426Question Mark
    Overlapping variant regions from other studies: 91 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):77,030,086-77,037,743Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6829277Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr777,400,76977,408,426
    nsv6829277RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr777,030,08677,037,743

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18547843deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18547843Submitted genomicNC_000007.14:g.774
    00769_77408426del
    GRCh38 (hg38)NC_000007.14Chr777,400,76977,408,426
    nssv18547843RemappedPerfectNC_000007.13:g.770
    30086_77037743del
    GRCh37.p13First PassNC_000007.13Chr777,030,08677,037,743

    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)
    nssv185478437e-062276264
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