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nsv6792463

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,345

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 23 studies. See in: genome view    
    Submitted genomic24,240,924-24,244,268Question Mark
    Overlapping variant regions from other studies: 82 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):24,241,152-24,244,496Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6792463Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr624,240,92424,244,268
    nsv6792463RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr624,241,15224,244,496

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18524240deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18524240Submitted genomicNC_000006.12:g.242
    40924_24244268del
    GRCh38 (hg38)NC_000006.12Chr624,240,92424,244,268
    nssv18524240RemappedPerfectNC_000006.11:g.242
    41152_24244496del
    GRCh37.p13First PassNC_000006.11Chr624,241,15224,244,496

    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)
    nssv185242404e-061275974
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