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nsv6668875

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:795,151

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1989 SVs from 79 studies. See in: genome view    
    Submitted genomic230,482,037-231,277,187Question Mark
    Overlapping variant regions from other studies: 1992 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):230,617,783-231,412,933Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6668875Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1230,482,037231,277,187
    nsv6668875RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1230,617,783231,412,933

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18608792duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18608792Submitted genomicNC_000001.11:g.230
    482037_231277187du
    p
    GRCh38 (hg38)NC_000001.11Chr1230,482,037231,277,187
    nssv18608792RemappedPerfectNC_000001.10:g.230
    617783_231412933du
    p
    GRCh37.p13First PassNC_000001.10Chr1230,617,783231,412,933

    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)
    nssv186087922.1e-056275450
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