U.S. flag

An official website of the United States government

nsv6949537

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,868

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 27 studies. See in: genome view    
    Submitted genomic45,238,632-45,246,499Question Mark
    Overlapping variant regions from other studies: 144 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):45,812,767-45,820,634Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6949537Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1345,238,63245,246,499
    nsv6949537RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1345,812,76745,820,634

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18378097deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18378097Submitted genomicNC_000013.11:g.452
    38632_45246499del
    GRCh38 (hg38)NC_000013.11Chr1345,238,63245,246,499
    nssv18378097RemappedPerfectNC_000013.10:g.458
    12767_45820634del
    GRCh37.p13First PassNC_000013.10Chr1345,812,76745,820,634

    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)
    nssv183780974e-061275976
    Support Center