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nsv7052838

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view    
    Submitted genomic174,787,987-174,788,051Question Mark
    Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):174,505,777-174,505,841Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052838Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3174,787,987174,788,051
    nsv7052838RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3174,505,777174,505,841

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769595inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769595Submitted genomicNC_000003.12:g.174
    787987_174788051in
    v
    GRCh38 (hg38)NC_000003.12Chr3174,787,987174,788,051
    nssv18769595RemappedPerfectNC_000003.11:g.174
    505777_174505841in
    v
    GRCh37.p13First PassNC_000003.11Chr3174,505,777174,505,841

    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)
    nssv187695951.1e-053276216
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