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nsv6926745

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,304

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
    Submitted genomic6,680,484-6,683,787Question Mark
    Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):6,789,650-6,792,953Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6926745Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr126,680,4846,683,787
    nsv6926745RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr126,789,6506,792,953

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18372037deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18372037Submitted genomicNC_000012.12:g.668
    0484_6683787del
    GRCh38 (hg38)NC_000012.12Chr126,680,4846,683,787
    nssv18372037RemappedPerfectNC_000012.11:g.678
    9650_6792953del
    GRCh37.p13First PassNC_000012.11Chr126,789,6506,792,953

    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)
    nssv183720374e-061274014
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