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nsv6437487

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:507,218

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2642 SVs from 109 studies. See in: genome view    
    Submitted genomic5,568,264-6,075,481Question Mark
    Overlapping variant regions from other studies: 2642 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):5,589,494-6,096,711Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6437487Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr115,568,2646,075,481
    nsv6437487RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr115,589,4946,096,711

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18187933duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18187933Submitted genomicNC_000011.10:g.556
    8264_6075481dup
    GRCh38 (hg38)NC_000011.10Chr115,568,2646,075,481
    nssv18187933RemappedPerfectNC_000011.9:g.5589
    494_6096711dup
    GRCh37.p13First PassNC_000011.9Chr115,589,4946,096,711

    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)
    nssv18187933<0.001239294
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