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nsv7057430

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:694,734

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2443 SVs from 101 studies. See in: genome view    
    Submitted genomic94,454,367-95,149,100Question Mark
    Overlapping variant regions from other studies: 2362 SVs from 101 studies. See in: genome view    
    Remapped(Score: Pass):95,164,085-95,680,543Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057430Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr694,454,36795,149,100
    nsv7057430RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr695,164,08595,680,543

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781288inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781288Submitted genomicNC_000006.12:g.944
    54367_95149100inv
    GRCh38 (hg38)NC_000006.12Chr694,454,36795,149,100
    nssv18781288RemappedPassNC_000006.11:g.951
    64085_95680543inv
    GRCh37.p13First PassNC_000006.11Chr695,164,08595,680,543

    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)
    nssv187812884e-061276268
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