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nsv7052448

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,016

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 189 SVs from 36 studies. See in: genome view    
    Submitted genomic65,000,823-65,039,838Question Mark
    Overlapping variant regions from other studies: 189 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):65,227,957-65,266,972Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052448Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr265,000,82365,039,838
    nsv7052448RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr265,227,95765,266,972

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768956inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768956Submitted genomicNC_000002.12:g.650
    00823_65039838inv
    GRCh38 (hg38)NC_000002.12Chr265,000,82365,039,838
    nssv18768956RemappedPerfectNC_000002.11:g.652
    27957_65266972inv
    GRCh37.p13First PassNC_000002.11Chr265,227,95765,266,972

    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)
    nssv187689564e-061276268
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