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nsv7049314

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,429,999

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3507 SVs from 111 studies. See in: genome view    
    Submitted genomic97,164,836-98,594,834Question Mark
    Overlapping variant regions from other studies: 3534 SVs from 111 studies. See in: genome view    
    Remapped(Score: Good):97,830,573-99,211,297Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7049314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr297,164,83698,594,834
    nsv7049314RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr297,830,57399,211,297

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18770066inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18770066Submitted genomicNC_000002.12:g.971
    64836_98594834inv
    GRCh38 (hg38)NC_000002.12Chr297,164,83698,594,834
    nssv18770066RemappedGoodNC_000002.11:g.978
    30573_99211297inv
    GRCh37.p13First PassNC_000002.11Chr297,830,57399,211,297

    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)
    nssv187700664e-061276268
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