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nsv7061712

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70,383

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 245 SVs from 39 studies. See in: genome view    
    Submitted genomic59,503,799-59,574,181Question Mark
    Overlapping variant regions from other studies: 245 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):59,271,272-59,341,654Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061712Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1159,503,79959,574,181
    nsv7061712RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1159,271,27259,341,654

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731878inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731878Submitted genomicNC_000011.10:g.595
    03799_59574181inv
    GRCh38 (hg38)NC_000011.10Chr1159,503,79959,574,181
    nssv18731878RemappedPerfectNC_000011.9:g.5927
    1272_59341654inv
    GRCh37.p13First PassNC_000011.9Chr1159,271,27259,341,654

    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)
    nssv187318784e-061276268
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