U.S. flag

An official website of the United States government

nsv6953676

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:195,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 570 SVs from 58 studies. See in: genome view    
    Submitted genomic53,644,001-53,839,500Question Mark
    Overlapping variant regions from other studies: 570 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):54,218,136-54,413,635Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6953676Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1353,644,00153,839,500
    nsv6953676RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1354,218,13654,413,635

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18378874deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18378874Submitted genomicNC_000013.11:g.536
    44001_53839500del
    GRCh38 (hg38)NC_000013.11Chr1353,644,00153,839,500
    nssv18378874RemappedPerfectNC_000013.10:g.542
    18136_54413635del
    GRCh37.p13First PassNC_000013.10Chr1354,218,13654,413,635

    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)
    nssv183788744e-061276216
    Support Center