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nsv7077159

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,311

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 215 SVs from 29 studies. See in: genome view    
    Submitted genomic127,071,925-127,088,235Question Mark
    Overlapping variant regions from other studies: 215 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):128,870,189-128,886,499Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077159Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10127,071,925127,088,235
    nsv7077159RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10128,870,189128,886,499

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743429inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743429Submitted genomicNC_000010.11:g.127
    071925_127088235in
    v
    GRCh38 (hg38)NC_000010.11Chr10127,071,925127,088,235
    nssv18743429RemappedPerfectNC_000010.10:g.128
    870189_128886499in
    v
    GRCh37.p13First PassNC_000010.10Chr10128,870,189128,886,499

    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)
    nssv187434292.1e-056274734
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