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nsv7048727

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,069,411

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7260 SVs from 107 studies. See in: genome view    
    Submitted genomic231,257,209-234,326,619Question Mark
    Overlapping variant regions from other studies: 7263 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):231,392,955-234,462,365Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048727Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,257,209234,326,619
    nsv7048727RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,392,955234,462,365

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758653inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758653Submitted genomicNC_000001.11:g.231
    257209_234326619in
    v
    GRCh38 (hg38)NC_000001.11Chr1231,257,209234,326,619
    nssv18758653RemappedPerfectNC_000001.10:g.231
    392955_234462365in
    v
    GRCh37.p13First PassNC_000001.10Chr1231,392,955234,462,365

    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)
    nssv187586534e-061276268
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