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nsv7038753

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:219,063

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 524 SVs from 62 studies. See in: genome view    
    Submitted genomic142,885,811-143,104,873Question Mark
    Overlapping variant regions from other studies: 499 SVs from 61 studies. See in: genome view    
    Remapped(Score: Good):142,583,556-142,801,966Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038753Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7142,885,811143,104,873
    nsv7038753RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7142,583,556142,801,966

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781377inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781377Submitted genomicNC_000007.14:g.142
    885811_143104873in
    v
    GRCh38 (hg38)NC_000007.14Chr7142,885,811143,104,873
    nssv18781377RemappedGoodNC_000007.13:g.142
    583556_142801966in
    v
    GRCh37.p13First PassNC_000007.13Chr7142,583,556142,801,966

    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)
    nssv187813777e-062275636
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