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nsv6894989

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,750

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 19 studies. See in: genome view    
    Submitted genomic99,606,803-99,609,552Question Mark
    Overlapping variant regions from other studies: 78 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):101,366,560-101,369,309Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6894989Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1099,606,80399,609,552
    nsv6894989RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10101,366,560101,369,309

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18341753deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18341753Submitted genomicNC_000010.11:g.996
    06803_99609552del
    GRCh38 (hg38)NC_000010.11Chr1099,606,80399,609,552
    nssv18341753RemappedPerfectNC_000010.10:g.101
    366560_101369309de
    l
    GRCh37.p13First PassNC_000010.10Chr10101,366,560101,369,309

    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)
    nssv183417534e-061275814
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