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nsv7064833

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,495

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 36 studies. See in: genome view    
    Submitted genomic96,212,664-96,224,158Question Mark
    Overlapping variant regions from other studies: 117 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):96,679,001-96,690,495Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064833Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1496,212,66496,224,158
    nsv7064833RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1496,679,00196,690,495

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755388inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755388Submitted genomicNC_000014.9:g.9621
    2664_96224158inv
    GRCh38 (hg38)NC_000014.9Chr1496,212,66496,224,158
    nssv18755388RemappedPerfectNC_000014.8:g.9667
    9001_96690495inv
    GRCh37.p13First PassNC_000014.8Chr1496,679,00196,690,495

    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)
    nssv187553880.004952274280
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