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nsv7052066

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,403,278

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9948 SVs from 117 studies. See in: genome view    
    Submitted genomic4,379,650-7,782,927Question Mark
    Overlapping variant regions from other studies: 9957 SVs from 117 studies. See in: genome view    
    Remapped(Score: Perfect):4,439,710-7,842,987Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052066Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr14,379,6507,782,927
    nsv7052066RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr14,439,7107,842,987

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760997inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760997Submitted genomicNC_000001.11:g.437
    9650_7782927inv
    GRCh38 (hg38)NC_000001.11Chr14,379,6507,782,927
    nssv18760997RemappedPerfectNC_000001.10:g.443
    9710_7842987inv
    GRCh37.p13First PassNC_000001.10Chr14,439,7107,842,987

    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)
    nssv187609974e-061276268
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