U.S. flag

An official website of the United States government

nsv7070223

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:886,569

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2519 SVs from 87 studies. See in: genome view    
    Submitted genomic61,482,736-62,369,304Question Mark
    Overlapping variant regions from other studies: 2519 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):59,560,097-60,446,665Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070223Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1761,482,73662,369,304
    nsv7070223RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1759,560,09760,446,665

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758488inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758488Submitted genomicNC_000017.11:g.614
    82736_62369304inv
    GRCh38 (hg38)NC_000017.11Chr1761,482,73662,369,304
    nssv18758488RemappedPerfectNC_000017.10:g.595
    60097_60446665inv
    GRCh37.p13First PassNC_000017.10Chr1759,560,09760,446,665

    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)
    nssv187584884e-061276268
    Support Center