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nsv6644694

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,754

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 29 studies. See in: genome view    
    Submitted genomic171,614,779-171,627,532Question Mark
    Overlapping variant regions from other studies: 176 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):171,583,919-171,596,672Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6644694Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1171,614,779171,627,532
    nsv6644694RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1171,583,919171,596,672

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18364108deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18364108Submitted genomicNC_000001.11:g.171
    614779_171627532de
    l
    GRCh38 (hg38)NC_000001.11Chr1171,614,779171,627,532
    nssv18364108RemappedPerfectNC_000001.10:g.171
    583919_171596672de
    l
    GRCh37.p13First PassNC_000001.10Chr1171,583,919171,596,672

    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)
    nssv183641084e-061276214
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