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nsv6330507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 27 studies. See in: genome view    
    Submitted genomic153,595,699-153,606,298Question Mark
    Overlapping variant regions from other studies: 139 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):153,568,175-153,578,774Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6330507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1153,595,699153,606,298
    nsv6330507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1153,568,175153,578,774

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18051988deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18051988Submitted genomicNC_000001.11:g.153
    595699_153606298de
    l
    GRCh38 (hg38)NC_000001.11Chr1153,595,699153,606,298
    nssv18051988RemappedPerfectNC_000001.10:g.153
    568175_153578774de
    l
    GRCh37.p13First PassNC_000001.10Chr1153,568,175153,578,774

    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)
    nssv18051988<0.001139186
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