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nsv7053774

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,601

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view    
    Submitted genomic228,147,848-228,150,448Question Mark
    Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):229,012,564-229,015,164Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053774Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,147,848228,150,448
    nsv7053774RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2229,012,564229,015,164

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767677inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767677Submitted genomicNC_000002.12:g.228
    147848_228150448in
    v
    GRCh38 (hg38)NC_000002.12Chr2228,147,848228,150,448
    nssv18767677RemappedPerfectNC_000002.11:g.229
    012564_229015164in
    v
    GRCh37.p13First PassNC_000002.11Chr2229,012,564229,015,164

    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)
    nssv187676774e-061276268
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