U.S. flag

An official website of the United States government

nsv7073486

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,118,124

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9140 SVs from 125 studies. See in: genome view    
    Submitted genomic15,622,817-18,740,940Question Mark
    Overlapping variant regions from other studies: 9140 SVs from 125 studies. See in: genome view    
    Remapped(Score: Perfect):15,526,131-18,644,253Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073486Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1715,622,81718,740,940
    nsv7073486RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1715,526,13118,644,253

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756156inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756156Submitted genomicNC_000017.11:g.156
    22817_18740940inv
    GRCh38 (hg38)NC_000017.11Chr1715,622,81718,740,940
    nssv18756156RemappedPerfectNC_000017.10:g.155
    26131_18644253inv
    GRCh37.p13First PassNC_000017.10Chr1715,526,13118,644,253

    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)
    nssv18756156<0.001168274144
    Support Center