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nsv7055907

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:136,295

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 887 SVs from 73 studies. See in: genome view    
    Submitted genomic186,235,011-186,371,305Question Mark
    Overlapping variant regions from other studies: 887 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):187,156,165-187,292,459Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055907Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4186,235,011186,371,305
    nsv7055907RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4187,156,165187,292,459

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774048inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774048Submitted genomicNC_000004.12:g.186
    235011_186371305in
    v
    GRCh38 (hg38)NC_000004.12Chr4186,235,011186,371,305
    nssv18774048RemappedPerfectNC_000004.11:g.187
    156165_187292459in
    v
    GRCh37.p13First PassNC_000004.11Chr4187,156,165187,292,459

    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)
    nssv187740484e-061276268
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