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nsv7062606

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:922,390

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3064 SVs from 83 studies. See in: genome view    
    Submitted genomic10,024,335-10,946,724Question Mark
    Overlapping variant regions from other studies: 3064 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):10,135,011-11,057,400Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062606Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1910,024,33510,946,724
    nsv7062606RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1910,135,01111,057,400

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759695inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759695Submitted genomicNC_000019.10:g.100
    24335_10946724inv
    GRCh38 (hg38)NC_000019.10Chr1910,024,33510,946,724
    nssv18759695RemappedPerfectNC_000019.9:g.1013
    5011_11057400inv
    GRCh37.p13First PassNC_000019.9Chr1910,135,01111,057,400

    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)
    nssv187596954e-061276268
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