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nsv6857309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,074

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 186 SVs from 26 studies. See in: genome view    
    Submitted genomic30,560,464-30,578,537Question Mark
    Overlapping variant regions from other studies: 186 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):30,417,981-30,436,054Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6857309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr830,560,46430,578,537
    nsv6857309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr830,417,98130,436,054

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749608duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749608Submitted genomicNC_000008.11:g.305
    60464_30578537dup
    GRCh38 (hg38)NC_000008.11Chr830,560,46430,578,537
    nssv18749608RemappedPerfectNC_000008.10:g.304
    17981_30436054dup
    GRCh37.p13First PassNC_000008.10Chr830,417,98130,436,054

    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)
    nssv187496084e-061276144
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