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nsv7072891

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,667

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 222 SVs from 24 studies. See in: genome view    
    Submitted genomic129,760,723-129,766,389Question Mark
    Overlapping variant regions from other studies: 222 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):131,558,987-131,564,653Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072891Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10129,760,723129,766,389
    nsv7072891RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10131,558,987131,564,653

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18741270inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18741270Submitted genomicNC_000010.11:g.129
    760723_129766389in
    v
    GRCh38 (hg38)NC_000010.11Chr10129,760,723129,766,389
    nssv18741270RemappedPerfectNC_000010.10:g.131
    558987_131564653in
    v
    GRCh37.p13First PassNC_000010.10Chr10131,558,987131,564,653

    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)
    nssv187412704e-061276268
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