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nsv6907749

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,525

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
    Submitted genomic73,028,119-73,031,643Question Mark
    Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):72,739,164-72,742,688Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6907749Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1173,028,11973,031,643
    nsv6907749RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1172,739,16472,742,688

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18352325deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18352325Submitted genomicNC_000011.10:g.730
    28119_73031643del
    GRCh38 (hg38)NC_000011.10Chr1173,028,11973,031,643
    nssv18352325RemappedPerfectNC_000011.9:g.7273
    9164_72742688del
    GRCh37.p13First PassNC_000011.9Chr1172,739,16472,742,688

    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)
    nssv18352325<0.00149275570
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