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nsv6909127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,661

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 30 studies. See in: genome view    
    Submitted genomic64,917,822-64,924,482Question Mark
    Overlapping variant regions from other studies: 101 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):64,685,294-64,691,954Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6909127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1164,917,82264,924,482
    nsv6909127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1164,685,29464,691,954

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351969deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351969Submitted genomicNC_000011.10:g.649
    17822_64924482del
    GRCh38 (hg38)NC_000011.10Chr1164,917,82264,924,482
    nssv18351969RemappedPerfectNC_000011.9:g.6468
    5294_64691954del
    GRCh37.p13First PassNC_000011.9Chr1164,685,29464,691,954

    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)
    nssv183519694e-061276096
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