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nsv6948633

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:433,475

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1540 SVs from 76 studies. See in: genome view    
    Submitted genomic45,036,674-45,470,148Question Mark
    Overlapping variant regions from other studies: 1540 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):45,610,809-46,044,283Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6948633Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1345,036,67445,470,148
    nsv6948633RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1345,610,80946,044,283

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18604286duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18604286Submitted genomicNC_000013.11:g.450
    36674_45470148dup
    GRCh38 (hg38)NC_000013.11Chr1345,036,67445,470,148
    nssv18604286RemappedPerfectNC_000013.10:g.456
    10809_46044283dup
    GRCh37.p13First PassNC_000013.10Chr1345,610,80946,044,283

    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)
    nssv186042861.1e-053275824
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