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nsv6905961

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:351,868

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1147 SVs from 86 studies. See in: genome view    
    Submitted genomic56,527,330-56,879,197Question Mark
    Overlapping variant regions from other studies: 1149 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):56,294,806-56,646,673Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6905961Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1156,527,33056,879,197
    nsv6905961RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1156,294,80656,646,673

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351693deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351693Submitted genomicNC_000011.10:g.565
    27330_56879197del
    GRCh38 (hg38)NC_000011.10Chr1156,527,33056,879,197
    nssv18351693RemappedPerfectNC_000011.9:g.5629
    4806_56646673del
    GRCh37.p13First PassNC_000011.9Chr1156,294,80656,646,673

    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)
    nssv183516932.1e-056274630
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