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nsv7043050

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:647,661

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2813 SVs from 95 studies. See in: genome view    
    Submitted genomic246,982,942-247,630,602Question Mark
    Overlapping variant regions from other studies: 2816 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):247,146,244-247,793,904Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043050Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1246,982,942247,630,602
    nsv7043050RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1247,146,244247,793,904

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759493inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759493Submitted genomicNC_000001.11:g.246
    982942_247630602in
    v
    GRCh38 (hg38)NC_000001.11Chr1246,982,942247,630,602
    nssv18759493RemappedPerfectNC_000001.10:g.247
    146244_247793904in
    v
    GRCh37.p13First PassNC_000001.10Chr1247,146,244247,793,904

    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)
    nssv187594934e-061276266
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