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nsv7073334

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79,328

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 369 SVs from 55 studies. See in: genome view    
    Submitted genomic48,958,315-49,037,642Question Mark
    Overlapping variant regions from other studies: 369 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):49,461,572-49,540,899Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073334Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,958,31549,037,642
    nsv7073334RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,461,57249,540,899

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760848inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760848Submitted genomicNC_000019.10:g.489
    58315_49037642inv
    GRCh38 (hg38)NC_000019.10Chr1948,958,31549,037,642
    nssv18760848RemappedPerfectNC_000019.9:g.4946
    1572_49540899inv
    GRCh37.p13First PassNC_000019.9Chr1949,461,57249,540,899

    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)
    nssv187608484e-060276268
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