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nsv6987172

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,492

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 28 studies. See in: genome view    
    Submitted genomic75,118,291-75,122,782Question Mark
    Overlapping variant regions from other studies: 148 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):73,114,386-73,118,877Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6987172Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,118,29175,122,782
    nsv6987172RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,114,38673,118,877

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18415206deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18415206Submitted genomicNC_000017.11:g.751
    18291_75122782del
    GRCh38 (hg38)NC_000017.11Chr1775,118,29175,122,782
    nssv18415206RemappedPerfectNC_000017.10:g.731
    14386_73118877del
    GRCh37.p13First PassNC_000017.10Chr1773,114,38673,118,877

    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)
    nssv184152061.8e-055275800
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