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nsv7038964

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 22 studies. See in: genome view    
    Submitted genomic223,741,216-223,741,233Question Mark
    Overlapping variant regions from other studies: 148 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):223,928,918-223,928,935Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038964Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1223,741,216223,741,233
    nsv7038964RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1223,928,918223,928,935

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761186inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761186Submitted genomicNC_000001.11:g.223
    741216_223741233in
    v
    GRCh38 (hg38)NC_000001.11Chr1223,741,216223,741,233
    nssv18761186RemappedPerfectNC_000001.10:g.223
    928918_223928935in
    v
    GRCh37.p13First PassNC_000001.10Chr1223,928,918223,928,935

    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)
    nssv187611864e-060276262
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