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nsv6668127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,594

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 23 studies. See in: genome view    
    Submitted genomic229,521,868-229,527,461Question Mark
    Overlapping variant regions from other studies: 146 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):229,657,615-229,663,208Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6668127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1229,521,868229,527,461
    nsv6668127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1229,657,615229,663,208

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18370196deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18370196Submitted genomicNC_000001.11:g.229
    521868_229527461de
    l
    GRCh38 (hg38)NC_000001.11Chr1229,521,868229,527,461
    nssv18370196RemappedPerfectNC_000001.10:g.229
    657615_229663208de
    l
    GRCh37.p13First PassNC_000001.10Chr1229,657,615229,663,208

    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)
    nssv183701964e-061276198
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