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nsv6965813

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:239,733

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 859 SVs from 74 studies. See in: genome view    
    Submitted genomic28,730,365-28,970,097Question Mark
    Overlapping variant regions from other studies: 859 SVs from 75 studies. See in: genome view    
    Remapped(Score: Pass):28,975,511-29,262,300Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6965813Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1528,730,36528,970,097
    nsv6965813RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1528,975,51129,262,300

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617906duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617906Submitted genomicNC_000015.10:g.287
    30365_28970097dup
    GRCh38 (hg38)NC_000015.10Chr1528,730,36528,970,097
    nssv18617906RemappedPassNC_000015.9:g.2897
    5511_29262300dup
    GRCh37.p13First PassNC_000015.9Chr1528,975,51129,262,300

    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)
    nssv186179067e-062275352
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