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nsv6507191

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,162

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 355 SVs from 49 studies. See in: genome view    
    Submitted genomic29,592,522-29,596,683Question Mark
    Overlapping variant regions from other studies: 355 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):29,603,843-29,608,004Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6507191Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1629,592,52229,596,683
    nsv6507191RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1629,603,84329,608,004

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18029101deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18029101Submitted genomicNC_000016.10:g.295
    92522_29596683del
    GRCh38 (hg38)NC_000016.10Chr1629,592,52229,596,683
    nssv18029101RemappedPerfectNC_000016.9:g.2960
    3843_29608004del
    GRCh37.p13First PassNC_000016.9Chr1629,603,84329,608,004

    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)
    nssv18029101<0.001338996
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