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nsv7067170

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,240,666

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11927 SVs from 119 studies. See in: genome view    
    Submitted genomic70,126,591-74,367,256Question Mark
    Overlapping variant regions from other studies: 11927 SVs from 119 studies. See in: genome view    
    Remapped(Score: Perfect):70,160,494-74,401,154Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067170Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1670,126,59174,367,256
    nsv7067170RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1670,160,49474,401,154

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758210inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758210Submitted genomicNC_000016.10:g.701
    26591_74367256inv
    GRCh38 (hg38)NC_000016.10Chr1670,126,59174,367,256
    nssv18758210RemappedPerfectNC_000016.9:g.7016
    0494_74401154inv
    GRCh37.p13First PassNC_000016.9Chr1670,160,49474,401,154

    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)
    nssv187582104e-061276266
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