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nsv7064889

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,267,566

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 12704 SVs from 115 studies. See in: genome view    
    Submitted genomic41,632,756-44,900,321Question Mark
    Overlapping variant regions from other studies: 12785 SVs from 115 studies. See in: genome view    
    Remapped(Score: Good):43,052,916-46,320,236Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064889Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2141,632,75644,900,321
    nsv7064889RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2143,052,91646,320,236

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762137inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762137Submitted genomicNC_000021.9:g.4163
    2756_44900321inv
    GRCh38 (hg38)NC_000021.9Chr2141,632,75644,900,321
    nssv18762137RemappedGoodNC_000021.8:g.4305
    2916_46320236inv
    GRCh37.p13First PassNC_000021.8Chr2143,052,91646,320,236

    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)
    nssv187621374e-061276266
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