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nsv7048323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:89

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 18 studies. See in: genome view    
    Submitted genomic163,200,695-163,200,783Question Mark
    Overlapping variant regions from other studies: 111 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):163,170,485-163,170,573Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1163,200,695163,200,783
    nsv7048323RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1163,170,485163,170,573

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739367inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739367Submitted genomicNC_000001.11:g.163
    200695_163200783in
    v
    GRCh38 (hg38)NC_000001.11Chr1163,200,695163,200,783
    nssv18739367RemappedPerfectNC_000001.10:g.163
    170485_163170573in
    v
    GRCh37.p13First PassNC_000001.10Chr1163,170,485163,170,573

    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)
    nssv187393674e-061276238
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