U.S. flag

An official website of the United States government

nsv7065519

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,579

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 22 studies. See in: genome view    
    Submitted genomic65,299,116-65,303,694Question Mark
    Overlapping variant regions from other studies: 93 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):65,333,019-65,337,597Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065519Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1665,299,11665,303,694
    nsv7065519RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1665,333,01965,337,597

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758141inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758141Submitted genomicNC_000016.10:g.652
    99116_65303694inv
    GRCh38 (hg38)NC_000016.10Chr1665,299,11665,303,694
    nssv18758141RemappedPerfectNC_000016.9:g.6533
    3019_65337597inv
    GRCh37.p13First PassNC_000016.9Chr1665,333,01965,337,597

    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)
    nssv187581414e-061276220
    Support Center