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nsv7052556

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 66 SVs from 15 studies. See in: genome view    
    Submitted genomic170,680,318-170,680,378Question Mark
    Overlapping variant regions from other studies: 66 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):170,107,322-170,107,382Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052556Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5170,680,318170,680,378
    nsv7052556RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5170,107,322170,107,382

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776159inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776159Submitted genomicNC_000005.10:g.170
    680318_170680378in
    v
    GRCh38 (hg38)NC_000005.10Chr5170,680,318170,680,378
    nssv18776159RemappedPerfectNC_000005.9:g.1701
    07322_170107382inv
    GRCh37.p13First PassNC_000005.9Chr5170,107,322170,107,382

    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)
    nssv187761594e-061276268
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