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nsv7048114

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,416,325

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 21383 SVs from 130 studies. See in: genome view    
    Submitted genomic76,979,006-85,395,330Question Mark
    Overlapping variant regions from other studies: 21382 SVs from 130 studies. See in: genome view    
    Remapped(Score: Perfect):76,608,323-85,024,646Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048114Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr776,979,00685,395,330
    nsv7048114RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr776,608,32385,024,646

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781986inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781986Submitted genomicNC_000007.14:g.769
    79006_85395330inv
    GRCh38 (hg38)NC_000007.14Chr776,979,00685,395,330
    nssv18781986RemappedPerfectNC_000007.13:g.766
    08323_85024646inv
    GRCh37.p13First PassNC_000007.13Chr776,608,32385,024,646

    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)
    nssv187819867e-062274460
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