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nsv7056676

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,577

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 236 SVs from 55 studies. See in: genome view    
    Submitted genomic148,173,476-148,175,052Question Mark
    Overlapping variant regions from other studies: 236 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):147,553,039-147,554,615Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056676Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,173,476148,175,052
    nsv7056676RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,553,039147,554,615

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774282inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774282Submitted genomicNC_000005.10:g.148
    173476_148175052in
    v
    GRCh38 (hg38)NC_000005.10Chr5148,173,476148,175,052
    nssv18774282RemappedPerfectNC_000005.9:g.1475
    53039_147554615inv
    GRCh37.p13First PassNC_000005.9Chr5147,553,039147,554,615

    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)
    nssv187742820.453108564240130
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