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nsv6643593

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,930

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Submitted genomic161,854,561-161,858,490Question Mark
    Overlapping variant regions from other studies: 125 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):161,824,351-161,828,280Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643593Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1161,854,561161,858,490
    nsv6643593RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1161,824,351161,828,280

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18363517deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18363517Submitted genomicNC_000001.11:g.161
    854561_161858490de
    l
    GRCh38 (hg38)NC_000001.11Chr1161,854,561161,858,490
    nssv18363517RemappedPerfectNC_000001.10:g.161
    824351_161828280de
    l
    GRCh37.p13First PassNC_000001.10Chr1161,824,351161,828,280

    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)
    nssv183635174e-061276046
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