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nsv7069320

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:395,916

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1664 SVs from 89 studies. See in: genome view    
    Submitted genomic89,699,356-90,095,271Question Mark
    Overlapping variant regions from other studies: 1664 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):89,432,524-89,828,439Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069320Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1189,699,35690,095,271
    nsv7069320RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1189,432,52489,828,439

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731716inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731716Submitted genomicNC_000011.10:g.896
    99356_90095271inv
    GRCh38 (hg38)NC_000011.10Chr1189,699,35690,095,271
    nssv18731716RemappedPerfectNC_000011.9:g.8943
    2524_89828439inv
    GRCh37.p13First PassNC_000011.9Chr1189,432,52489,828,439

    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)
    nssv187317167e-062274896
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