U.S. flag

An official website of the United States government

nsv6787762

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:246,857

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 900 SVs from 76 studies. See in: genome view    
    Submitted genomic27,694,542-27,941,398Question Mark
    Overlapping variant regions from other studies: 900 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):27,662,321-27,909,176Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6787762Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr627,694,54227,941,398
    nsv6787762RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr627,662,32127,909,176

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18714748duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18714748Submitted genomicNC_000006.12:g.276
    94542_27941398dup
    GRCh38 (hg38)NC_000006.12Chr627,694,54227,941,398
    nssv18714748RemappedPerfectNC_000006.11:g.276
    62321_27909176dup
    GRCh37.p13First PassNC_000006.11Chr627,662,32127,909,176

    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)
    nssv187147484e-061271610
    Support Center