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nsv6603505

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:138,842

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 476 SVs from 68 studies. See in: genome view    
    Submitted genomic133,810,537-133,949,378Question Mark
    Overlapping variant regions from other studies: 476 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):134,131,675-134,270,516Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6603505Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6133,810,537133,949,378
    nsv6603505RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6134,131,675134,270,516

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18215596duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18215596Submitted genomicNC_000006.12:g.133
    810537_133949378du
    p
    GRCh38 (hg38)NC_000006.12Chr6133,810,537133,949,378
    nssv18215596RemappedPerfectNC_000006.11:g.134
    131675_134270516du
    p
    GRCh37.p13First PassNC_000006.11Chr6134,131,675134,270,516

    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)
    nssv18215596<0.001439272
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