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nsv6798024

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,240

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 31 studies. See in: genome view    
    Submitted genomic17,950,069-17,953,308Question Mark
    Overlapping variant regions from other studies: 142 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):17,950,300-17,953,539Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6798024Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr617,950,06917,953,308
    nsv6798024RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr617,950,30017,953,539

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18526987deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18526987Submitted genomicNC_000006.12:g.179
    50069_17953308del
    GRCh38 (hg38)NC_000006.12Chr617,950,06917,953,308
    nssv18526987RemappedPerfectNC_000006.11:g.179
    50300_17953539del
    GRCh37.p13First PassNC_000006.11Chr617,950,30017,953,539

    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)
    nssv185269874e-061276062
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