U.S. flag

An official website of the United States government

nsv7047466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,664

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 254 SVs from 32 studies. See in: genome view    
    Submitted genomic245,522,858-245,532,521Question Mark
    Overlapping variant regions from other studies: 257 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):245,686,160-245,695,823Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047466Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1245,522,858245,532,521
    nsv7047466RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1245,686,160245,695,823

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759469inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759469Submitted genomicNC_000001.11:g.245
    522858_245532521in
    v
    GRCh38 (hg38)NC_000001.11Chr1245,522,858245,532,521
    nssv18759469RemappedPerfectNC_000001.10:g.245
    686160_245695823in
    v
    GRCh37.p13First PassNC_000001.10Chr1245,686,160245,695,823

    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)
    nssv187594694e-061276268
    Support Center