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nsv7038550

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:325,504

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1830 SVs from 108 studies. See in: genome view    
    Submitted genomic76,433,435-76,758,938Question Mark
    Overlapping variant regions from other studies: 1828 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):76,062,752-76,388,255Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038550Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr776,433,43576,758,938
    nsv7038550RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr776,062,75276,388,255

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781977inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781977Submitted genomicNC_000007.14:g.764
    33435_76758938inv
    GRCh38 (hg38)NC_000007.14Chr776,433,43576,758,938
    nssv18781977RemappedPerfectNC_000007.13:g.760
    62752_76388255inv
    GRCh37.p13First PassNC_000007.13Chr776,062,75276,388,255

    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)
    nssv187819774e-061276268
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