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nsv6678540

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,156

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 302 SVs from 48 studies. See in: genome view    
    Submitted genomic230,799,348-230,905,503Question Mark
    Overlapping variant regions from other studies: 302 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):231,664,063-231,770,218Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6678540Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2230,799,348230,905,503
    nsv6678540RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,664,063231,770,218

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18664962duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18664962Submitted genomicNC_000002.12:g.230
    799348_230905503du
    p
    GRCh38 (hg38)NC_000002.12Chr2230,799,348230,905,503
    nssv18664962RemappedPerfectNC_000002.11:g.231
    664063_231770218du
    p
    GRCh37.p13First PassNC_000002.11Chr2231,664,063231,770,218

    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)
    nssv186649621.1e-053275594
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