nsv6903036

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:116,847

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 386 SVs from 62 studies. See in: genome view    
    Submitted genomic56,420,634-56,537,480Question Mark
    Overlapping variant regions from other studies: 388 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):56,188,110-56,304,956Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6903036Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1156,420,63456,537,480
    nsv6903036RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1156,188,11056,304,956

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351683deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351683Submitted genomicNC_000011.10:g.564
    20634_56537480del
    GRCh38 (hg38)NC_000011.10Chr1156,420,63456,537,480
    nssv18351683RemappedPerfectNC_000011.9:g.5618
    8110_56304956del
    GRCh37.p13First PassNC_000011.9Chr1156,188,11056,304,956

    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)
    nssv183516837e-062276180
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