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nsv6643657

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 27 studies. See in: genome view    
    Submitted genomic163,251,001-163,269,000Question Mark
    Overlapping variant regions from other studies: 142 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):163,220,791-163,238,790Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643657Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1163,251,001163,269,000
    nsv6643657RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1163,220,791163,238,790

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18364479deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18364479Submitted genomicNC_000001.11:g.163
    251001_163269000de
    l
    GRCh38 (hg38)NC_000001.11Chr1163,251,001163,269,000
    nssv18364479RemappedPerfectNC_000001.10:g.163
    220791_163238790de
    l
    GRCh37.p13First PassNC_000001.10Chr1163,220,791163,238,790

    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)
    nssv183644794e-061276140
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