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nsv7076630

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,034,590

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2793 SVs from 82 studies. See in: genome view    
    Submitted genomic29,313,096-30,347,685Question Mark
    Overlapping variant regions from other studies: 2793 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):29,602,025-30,636,614Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076630Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1029,313,09630,347,685
    nsv7076630RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1029,602,02530,636,614

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18750818inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18750818Submitted genomicNC_000010.11:g.293
    13096_30347685inv
    GRCh38 (hg38)NC_000010.11Chr1029,313,09630,347,685
    nssv18750818RemappedPerfectNC_000010.10:g.296
    02025_30636614inv
    GRCh37.p13First PassNC_000010.10Chr1029,602,02530,636,614

    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)
    nssv187508187e-062273850
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