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nsv6667150

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,960

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 27 studies. See in: genome view    
    Submitted genomic210,148,456-210,153,415Question Mark
    Overlapping variant regions from other studies: 141 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):210,321,801-210,326,760Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6667150Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1210,148,456210,153,415
    nsv6667150RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1210,321,801210,326,760

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18366510deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18366510Submitted genomicNC_000001.11:g.210
    148456_210153415de
    l
    GRCh38 (hg38)NC_000001.11Chr1210,148,456210,153,415
    nssv18366510RemappedPerfectNC_000001.10:g.210
    321801_210326760de
    l
    GRCh37.p13First PassNC_000001.10Chr1210,321,801210,326,760

    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)
    nssv183665101.4e-054275998
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