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nsv6974656

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 478 SVs from 38 studies. See in: genome view    
    Submitted genomic23,632,501-23,648,400Question Mark
    Overlapping variant regions from other studies: 482 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):23,877,648-23,893,547Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6974656Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1523,632,50123,648,400
    nsv6974656RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1523,877,64823,893,547

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615970duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615970Submitted genomicNC_000015.10:g.236
    32501_23648400dup
    GRCh38 (hg38)NC_000015.10Chr1523,632,50123,648,400
    nssv18615970RemappedPerfectNC_000015.9:g.2387
    7648_23893547dup
    GRCh37.p13First PassNC_000015.9Chr1523,877,64823,893,547

    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)
    nssv186159704e-061274708
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