U.S. flag

An official website of the United States government

nsv6792679

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:160,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 548 SVs from 58 studies. See in: genome view    
    Submitted genomic42,936,101-43,096,800Question Mark
    Overlapping variant regions from other studies: 548 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):42,903,839-43,064,538Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6792679Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr642,936,10143,096,800
    nsv6792679RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr642,903,83943,064,538

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18716166duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18716166Submitted genomicNC_000006.12:g.429
    36101_43096800dup
    GRCh38 (hg38)NC_000006.12Chr642,936,10143,096,800
    nssv18716166RemappedPerfectNC_000006.11:g.429
    03839_43064538dup
    GRCh37.p13First PassNC_000006.11Chr642,903,83943,064,538

    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)
    nssv187161664e-061240268
    Support Center