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nsv7065010

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,779,243

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6855 SVs from 95 studies. See in: genome view    
    Submitted genomic32,699,822-35,479,064Question Mark
    Overlapping variant regions from other studies: 6855 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):32,988,750-35,767,992Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065010Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1032,699,82235,479,064
    nsv7065010RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1032,988,75035,767,992

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747799inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747799Submitted genomicNC_000010.11:g.326
    99822_35479064inv
    GRCh38 (hg38)NC_000010.11Chr1032,699,82235,479,064
    nssv18747799RemappedPerfectNC_000010.10:g.329
    88750_35767992inv
    GRCh37.p13First PassNC_000010.10Chr1032,988,75035,767,992

    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)
    nssv187477994e-061276268
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