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nsv6507777

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:411

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 38 studies. See in: genome view    
    Submitted genomic41,311,822-41,312,232Question Mark
    Overlapping variant regions from other studies: 127 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):41,604,020-41,604,430Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6507777Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1541,311,82241,312,232
    nsv6507777RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,604,02041,604,430

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18023665deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18023665Submitted genomicNC_000015.10:g.413
    11822_41312232del
    GRCh38 (hg38)NC_000015.10Chr1541,311,82241,312,232
    nssv18023665RemappedPerfectNC_000015.9:g.4160
    4020_41604430del
    GRCh37.p13First PassNC_000015.9Chr1541,604,02041,604,430

    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)
    nssv180236650.211688732718
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