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nsv6895424

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:410

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 18 studies. See in: genome view    
    Submitted genomic75,720,464-75,720,873Question Mark
    Overlapping variant regions from other studies: 92 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):77,480,222-77,480,631Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6895424Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1075,720,46475,720,873
    nsv6895424RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1077,480,22277,480,631

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586926duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586926Submitted genomicNC_000010.11:g.757
    20464_75720873dup
    GRCh38 (hg38)NC_000010.11Chr1075,720,46475,720,873
    nssv18586926RemappedPerfectNC_000010.10:g.774
    80222_77480631dup
    GRCh37.p13First PassNC_000010.10Chr1077,480,22277,480,631

    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)
    nssv185869268e-062241814
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