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nsv6480571

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 27 studies. See in: genome view    
    Submitted genomic60,970,801-60,975,600Question Mark
    Overlapping variant regions from other studies: 116 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):61,437,519-61,442,318Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6480571Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1460,970,80160,975,600
    nsv6480571RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1461,437,51961,442,318

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18190862duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18190862Submitted genomicNC_000014.9:g.6097
    0801_60975600dup
    GRCh38 (hg38)NC_000014.9Chr1460,970,80160,975,600
    nssv18190862RemappedPerfectNC_000014.8:g.6143
    7519_61442318dup
    GRCh37.p13First PassNC_000014.8Chr1461,437,51961,442,318

    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)
    nssv18190862<0.0011139202
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