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nsv7066336

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,983

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 24 studies. See in: genome view    
    Submitted genomic88,142,902-88,148,884Question Mark
    Overlapping variant regions from other studies: 127 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):88,686,133-88,692,115Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066336Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1588,142,90288,148,884
    nsv7066336RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1588,686,13388,692,115

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756084inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756084Submitted genomicNC_000015.10:g.881
    42902_88148884inv
    GRCh38 (hg38)NC_000015.10Chr1588,142,90288,148,884
    nssv18756084RemappedPerfectNC_000015.9:g.8868
    6133_88692115inv
    GRCh37.p13First PassNC_000015.9Chr1588,686,13388,692,115

    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)
    nssv187560844e-061276268
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