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nsv7051578

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:190,879

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 419 SVs from 47 studies. See in: genome view    
    Submitted genomic147,634,714-147,825,592Question Mark
    Overlapping variant regions from other studies: 419 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):147,014,277-147,205,155Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051578Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5147,634,714147,825,592
    nsv7051578RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,014,277147,205,155

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774273inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774273Submitted genomicNC_000005.10:g.147
    634714_147825592in
    v
    GRCh38 (hg38)NC_000005.10Chr5147,634,714147,825,592
    nssv18774273RemappedPerfectNC_000005.9:g.1470
    14277_147205155inv
    GRCh37.p13First PassNC_000005.9Chr5147,014,277147,205,155

    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)
    nssv187742734e-061276268
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