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nsv6860073

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:814

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 26 studies. See in: genome view    
    Submitted genomic128,817,343-128,818,156Question Mark
    Overlapping variant regions from other studies: 168 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):131,579,622-131,580,435Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6860073Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9128,817,343128,818,156
    nsv6860073RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9131,579,622131,580,435

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18562153deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18562153Submitted genomicNC_000009.12:g.128
    817343_128818156de
    l
    GRCh38 (hg38)NC_000009.12Chr9128,817,343128,818,156
    nssv18562153RemappedPerfectNC_000009.11:g.131
    579622_131580435de
    l
    GRCh37.p13First PassNC_000009.11Chr9131,579,622131,580,435

    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)
    nssv18562153<0.00155268916
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