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nsv7075000

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:572,915

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1205 SVs from 78 studies. See in: genome view    
    Submitted genomic50,218,729-50,791,643Question Mark
    Overlapping variant regions from other studies: 1209 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):51,978,489-52,551,403Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075000Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,218,72950,791,643
    nsv7075000RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1051,978,48952,551,403

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18735335inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18735335Submitted genomicNC_000010.11:g.502
    18729_50791643inv
    GRCh38 (hg38)NC_000010.11Chr1050,218,72950,791,643
    nssv18735335RemappedPerfectNC_000010.10:g.519
    78489_52551403inv
    GRCh37.p13First PassNC_000010.10Chr1051,978,48952,551,403

    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)
    nssv187353354e-061276268
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