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nsv6763778

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,730

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 31 studies. See in: genome view    
    Submitted genomic15,603,660-15,606,389Question Mark
    Overlapping variant regions from other studies: 190 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):15,603,769-15,606,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6763778Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr515,603,66015,606,389
    nsv6763778RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr515,603,76915,606,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18509425deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18509425Submitted genomicNC_000005.10:g.156
    03660_15606389del
    GRCh38 (hg38)NC_000005.10Chr515,603,66015,606,389
    nssv18509425RemappedPerfectNC_000005.9:g.1560
    3769_15606498del
    GRCh37.p13First PassNC_000005.9Chr515,603,76915,606,498

    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)
    nssv18509425<0.001162253354
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