U.S. flag

An official website of the United States government

nsv6666880

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,829

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 207 SVs from 37 studies. See in: genome view    
    Submitted genomic231,381,311-231,396,139Question Mark
    Overlapping variant regions from other studies: 210 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):231,517,057-231,531,885Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6666880Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,381,311231,396,139
    nsv6666880RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,517,057231,531,885

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18368534deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18368534Submitted genomicNC_000001.11:g.231
    381311_231396139de
    l
    GRCh38 (hg38)NC_000001.11Chr1231,381,311231,396,139
    nssv18368534RemappedPerfectNC_000001.10:g.231
    517057_231531885de
    l
    GRCh37.p13First PassNC_000001.10Chr1231,517,057231,531,885

    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)
    nssv183685344e-061276262
    Support Center