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nsv6879073

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:542

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 67 SVs from 12 studies. See in: genome view    
    Submitted genomic31,832,409-31,832,950Question Mark
    Overlapping variant regions from other studies: 67 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):32,121,337-32,121,878Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6879073Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1031,832,40931,832,950
    nsv6879073RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1032,121,33732,121,878

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18572039duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18572039Submitted genomicNC_000010.11:g.318
    32409_31832950dup
    GRCh38 (hg38)NC_000010.11Chr1031,832,40931,832,950
    nssv18572039RemappedPerfectNC_000010.10:g.321
    21337_32121878dup
    GRCh37.p13First PassNC_000010.10Chr1032,121,33732,121,878

    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)
    nssv185720392e-055244948
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