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nsv6704578

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46,926

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 294 SVs from 46 studies. See in: genome view    
    Submitted genomic9,886,882-9,933,807Question Mark
    Overlapping variant regions from other studies: 294 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):9,928,566-9,975,491Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6704578Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr39,886,8829,933,807
    nsv6704578RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr39,928,5669,975,491

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18680537duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18680537Submitted genomicNC_000003.12:g.988
    6882_9933807dup
    GRCh38 (hg38)NC_000003.12Chr39,886,8829,933,807
    nssv18680537RemappedPerfectNC_000003.11:g.992
    8566_9975491dup
    GRCh37.p13First PassNC_000003.11Chr39,928,5669,975,491

    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)
    nssv186805374e-061274642
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