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nsv6473414

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,930

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1715 SVs from 104 studies. See in: genome view    
    Submitted genomic7,798,959-7,905,888Question Mark
    Overlapping variant regions from other studies: 1715 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):7,951,555-8,058,484Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6473414Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,798,9597,905,888
    nsv6473414RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr127,951,5558,058,484

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18186418duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18186418Submitted genomicNC_000012.12:g.779
    8959_7905888dup
    GRCh38 (hg38)NC_000012.12Chr127,798,9597,905,888
    nssv18186418RemappedPerfectNC_000012.11:g.795
    1555_8058484dup
    GRCh37.p13First PassNC_000012.11Chr127,951,5558,058,484

    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)
    nssv18186418<0.0011923364
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