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nsv7063990

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,939

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 29 studies. See in: genome view    
    Submitted genomic88,154,736-88,179,674Question Mark
    Overlapping variant regions from other studies: 142 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):87,887,904-87,912,842Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063990Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1188,154,73688,179,674
    nsv7063990RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1187,887,90487,912,842

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18750239inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18750239Submitted genomicNC_000011.10:g.881
    54736_88179674inv
    GRCh38 (hg38)NC_000011.10Chr1188,154,73688,179,674
    nssv18750239RemappedPerfectNC_000011.9:g.8788
    7904_87912842inv
    GRCh37.p13First PassNC_000011.9Chr1187,887,90487,912,842

    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)
    nssv187502394e-061276268
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