nsv7067272

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:497,728

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1658 SVs from 87 studies. See in: genome view    
    Submitted genomic17,179,403-17,677,130Question Mark
    Overlapping variant regions from other studies: 1658 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):17,036,912-17,534,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067272Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr817,179,40317,677,130
    nsv7067272RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr817,036,91217,534,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782324inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782324Submitted genomicNC_000008.11:g.171
    79403_17677130inv
    GRCh38 (hg38)NC_000008.11Chr817,179,40317,677,130
    nssv18782324RemappedPerfectNC_000008.10:g.170
    36912_17534639inv
    GRCh37.p13First PassNC_000008.10Chr817,036,91217,534,639

    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)
    nssv187823244e-061276268
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