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nsv7044357

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,343,494

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5861 SVs from 107 studies. See in: genome view    
    Submitted genomic230,487,375-232,830,868Question Mark
    Overlapping variant regions from other studies: 5864 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):230,623,121-232,966,614Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044357Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1230,487,375232,830,868
    nsv7044357RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1230,623,121232,966,614

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758643inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758643Submitted genomicNC_000001.11:g.230
    487375_232830868in
    v
    GRCh38 (hg38)NC_000001.11Chr1230,487,375232,830,868
    nssv18758643RemappedPerfectNC_000001.10:g.230
    623121_232966614in
    v
    GRCh37.p13First PassNC_000001.10Chr1230,623,121232,966,614

    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)
    nssv187586434e-061276268
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