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nsv7052590

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,576,542

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10061 SVs from 111 studies. See in: genome view    
    Submitted genomic154,695,187-159,271,728Question Mark
    Overlapping variant regions from other studies: 10056 SVs from 111 studies. See in: genome view    
    Remapped(Score: Good):154,074,747-158,698,736Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052590Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5154,695,187159,271,728
    nsv7052590RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5154,074,747158,698,736

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774953inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774953Submitted genomicNC_000005.10:g.154
    695187_159271728in
    v
    GRCh38 (hg38)NC_000005.10Chr5154,695,187159,271,728
    nssv18774953RemappedGoodNC_000005.9:g.1540
    74747_158698736inv
    GRCh37.p13First PassNC_000005.9Chr5154,074,747158,698,736

    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)
    nssv187749534e-061276268
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