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nsv7065381

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,395,465

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 19282 SVs from 127 studies. See in: genome view    
    Submitted genomic83,674,811-92,070,275Question Mark
    Overlapping variant regions from other studies: 19284 SVs from 127 studies. See in: genome view    
    Remapped(Score: Perfect):85,434,567-93,830,032Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065381Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1083,674,81192,070,275
    nsv7065381RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1085,434,56793,830,032

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734206inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734206Submitted genomicNC_000010.11:g.836
    74811_92070275inv
    GRCh38 (hg38)NC_000010.11Chr1083,674,81192,070,275
    nssv18734206RemappedPerfectNC_000010.10:g.854
    34567_93830032inv
    GRCh37.p13First PassNC_000010.10Chr1085,434,56793,830,032

    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)
    nssv187342064e-061276268
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