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nsv6507361

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:186,801

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 673 SVs from 55 studies. See in: genome view    
    Submitted genomic43,844,289-44,031,089Question Mark
    Overlapping variant regions from other studies: 671 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):41,921,657-42,108,457Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6507361Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1743,844,28944,031,089
    nsv6507361RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1741,921,65742,108,457

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18194760duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18194760Submitted genomicNC_000017.11:g.438
    44289_44031089dup
    GRCh38 (hg38)NC_000017.11Chr1743,844,28944,031,089
    nssv18194760RemappedPerfectNC_000017.10:g.419
    21657_42108457dup
    GRCh37.p13First PassNC_000017.10Chr1741,921,65742,108,457

    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)
    nssv18194760<0.001139294
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