U.S. flag

An official website of the United States government

nsv6711219

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:201,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 814 SVs from 64 studies. See in: genome view    
    Submitted genomic11,626,401-11,828,000Question Mark
    Overlapping variant regions from other studies: 814 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):11,667,875-11,869,474Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6711219Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,626,40111,828,000
    nsv6711219RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,667,87511,869,474

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18669626duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18669626Submitted genomicNC_000003.12:g.116
    26401_11828000dup
    GRCh38 (hg38)NC_000003.12Chr311,626,40111,828,000
    nssv18669626RemappedPerfectNC_000003.11:g.116
    67875_11869474dup
    GRCh37.p13First PassNC_000003.11Chr311,667,87511,869,474

    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)
    nssv186696264e-061275362
    Support Center