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nsv7057058

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,812,109

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11108 SVs from 121 studies. See in: genome view    
    Submitted genomic165,065,528-168,877,636Question Mark
    Overlapping variant regions from other studies: 11108 SVs from 121 studies. See in: genome view    
    Remapped(Score: Perfect):165,986,680-169,798,787Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057058Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4165,065,528168,877,636
    nsv7057058RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4165,986,680169,798,787

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773144inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773144Submitted genomicNC_000004.12:g.165
    065528_168877636in
    v
    GRCh38 (hg38)NC_000004.12Chr4165,065,528168,877,636
    nssv18773144RemappedPerfectNC_000004.11:g.165
    986680_169798787in
    v
    GRCh37.p13First PassNC_000004.11Chr4165,986,680169,798,787

    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)
    nssv187731444e-061276268
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