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nsv6846293

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,416

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 29 studies. See in: genome view    
    Submitted genomic64,642,114-64,652,529Question Mark
    Overlapping variant regions from other studies: 133 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):65,554,671-65,565,086Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6846293Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr864,642,11464,652,529
    nsv6846293RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr865,554,67165,565,086

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18557979deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18557979Submitted genomicNC_000008.11:g.646
    42114_64652529del
    GRCh38 (hg38)NC_000008.11Chr864,642,11464,652,529
    nssv18557979RemappedPerfectNC_000008.10:g.655
    54671_65565086del
    GRCh37.p13First PassNC_000008.10Chr865,554,67165,565,086

    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)
    nssv185579794e-061276204
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