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nsv7042482

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,008

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 160 SVs from 39 studies. See in: genome view    
    Submitted genomic38,373,006-38,383,013Question Mark
    Overlapping variant regions from other studies: 160 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):38,412,607-38,422,614Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042482Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr738,373,00638,383,013
    nsv7042482RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr738,412,60738,422,614

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780697inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780697Submitted genomicNC_000007.14:g.383
    73006_38383013inv
    GRCh38 (hg38)NC_000007.14Chr738,373,00638,383,013
    nssv18780697RemappedPerfectNC_000007.13:g.384
    12607_38422614inv
    GRCh37.p13First PassNC_000007.13Chr738,412,60738,422,614

    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)
    nssv187806974e-061276268
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