U.S. flag

An official website of the United States government

nsv6941402

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:245,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 622 SVs from 69 studies. See in: genome view    
    Submitted genomic24,059,301-24,305,100Question Mark
    Overlapping variant regions from other studies: 626 SVs from 69 studies. See in: genome view    
    Remapped(Score: Good):24,528,510-24,774,306Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6941402Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1424,059,30124,305,100
    nsv6941402RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1424,528,51024,774,306

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611829duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611829Submitted genomicNC_000014.9:g.2405
    9301_24305100dup
    GRCh38 (hg38)NC_000014.9Chr1424,059,30124,305,100
    nssv18611829RemappedGoodNC_000014.8:g.2452
    8510_24774306dup
    GRCh37.p13First PassNC_000014.8Chr1424,528,51024,774,306

    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)
    nssv186118294e-061274446
    Support Center