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nsv7075933

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,181,370

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5723 SVs from 114 studies. See in: genome view    
    Submitted genomic27,763,634-29,945,003Question Mark
    Overlapping variant regions from other studies: 5763 SVs from 114 studies. See in: genome view    
    Remapped(Score: Good):28,008,780-30,237,206Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075933Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1527,763,63429,945,003
    nsv7075933RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1528,008,78030,237,206

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755962inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755962Submitted genomicNC_000015.10:g.277
    63634_29945003inv
    GRCh38 (hg38)NC_000015.10Chr1527,763,63429,945,003
    nssv18755962RemappedGoodNC_000015.9:g.2800
    8780_30237206inv
    GRCh37.p13First PassNC_000015.9Chr1528,008,78030,237,206

    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)
    nssv187559627e-062274880
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