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nsv7074385

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,914

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 30 studies. See in: genome view    
    Submitted genomic59,401,436-59,410,349Question Mark
    Overlapping variant regions from other studies: 132 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):59,693,635-59,702,548Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074385Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1559,401,43659,410,349
    nsv7074385RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,693,63559,702,548

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756323inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756323Submitted genomicNC_000015.10:g.594
    01436_59410349inv
    GRCh38 (hg38)NC_000015.10Chr1559,401,43659,410,349
    nssv18756323RemappedPerfectNC_000015.9:g.5969
    3635_59702548inv
    GRCh37.p13First PassNC_000015.9Chr1559,693,63559,702,548

    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)
    nssv187563234e-061276268
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