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nsv7042604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,279

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 19 studies. See in: genome view    
    Submitted genomic57,788,552-57,790,830Question Mark
    Overlapping variant regions from other studies: 112 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):58,254,224-58,256,502Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr157,788,55257,790,830
    nsv7042604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr158,254,22458,256,502

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761615inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761615Submitted genomicNC_000001.11:g.577
    88552_57790830inv
    GRCh38 (hg38)NC_000001.11Chr157,788,55257,790,830
    nssv18761615RemappedPerfectNC_000001.10:g.582
    54224_58256502inv
    GRCh37.p13First PassNC_000001.10Chr158,254,22458,256,502

    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)
    nssv187616154e-061276268
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