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nsv7048996

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,851

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 180 SVs from 29 studies. See in: genome view    
    Submitted genomic240,958,080-240,963,930Question Mark
    Overlapping variant regions from other studies: 183 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):241,121,380-241,127,230Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048996Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1240,958,080240,963,930
    nsv7048996RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1241,121,380241,127,230

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759414inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759414Submitted genomicNC_000001.11:g.240
    958080_240963930in
    v
    GRCh38 (hg38)NC_000001.11Chr1240,958,080240,963,930
    nssv18759414RemappedPerfectNC_000001.10:g.241
    121380_241127230in
    v
    GRCh37.p13First PassNC_000001.10Chr1241,121,380241,127,230

    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)
    nssv187594141.8e-055275452
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