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nsv7047502

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:230,932

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 574 SVs from 60 studies. See in: genome view    
    Submitted genomic37,299,925-37,530,856Question Mark
    Overlapping variant regions from other studies: 574 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):37,341,416-37,572,347Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047502Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr337,299,92537,530,856
    nsv7047502RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr337,341,41637,572,347

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771675inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771675Submitted genomicNC_000003.12:g.372
    99925_37530856inv
    GRCh38 (hg38)NC_000003.12Chr337,299,92537,530,856
    nssv18771675RemappedPerfectNC_000003.11:g.373
    41416_37572347inv
    GRCh37.p13First PassNC_000003.11Chr337,341,41637,572,347

    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)
    nssv187716751.8e-055276112
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