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nsv7072429

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,812

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 265 SVs from 48 studies. See in: genome view    
    Submitted genomic38,777,411-38,800,222Question Mark
    Overlapping variant regions from other studies: 265 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):39,268,051-39,290,862Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072429Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1938,777,41138,800,222
    nsv7072429RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1939,268,05139,290,862

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758625inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758625Submitted genomicNC_000019.10:g.387
    77411_38800222inv
    GRCh38 (hg38)NC_000019.10Chr1938,777,41138,800,222
    nssv18758625RemappedPerfectNC_000019.9:g.3926
    8051_39290862inv
    GRCh37.p13First PassNC_000019.9Chr1939,268,05139,290,862

    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)
    nssv187586254e-061276268
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