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nsv7072675

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:223,384

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 681 SVs from 65 studies. See in: genome view    
    Submitted genomic60,917,917-61,141,300Question Mark
    Overlapping variant regions from other studies: 681 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):60,685,389-60,908,772Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072675Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1160,917,91761,141,300
    nsv7072675RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1160,685,38960,908,772

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743595inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743595Submitted genomicNC_000011.10:g.609
    17917_61141300inv
    GRCh38 (hg38)NC_000011.10Chr1160,917,91761,141,300
    nssv18743595RemappedPerfectNC_000011.9:g.6068
    5389_60908772inv
    GRCh37.p13First PassNC_000011.9Chr1160,685,38960,908,772

    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)
    nssv187435954e-061276268
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