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nsv6549900

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,059,737

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7658 SVs from 115 studies. See in: genome view    
    Submitted genomic229,174,803-232,234,539Question Mark
    Overlapping variant regions from other studies: 7661 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):229,310,550-232,370,285Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6549900Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1229,174,803232,234,539
    nsv6549900RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1229,310,550232,370,285

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18250315inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18250315Submitted genomicNC_000001.11:g.229
    174803_232234539in
    v
    GRCh38 (hg38)NC_000001.11Chr1229,174,803232,234,539
    nssv18250315RemappedPerfectNC_000001.10:g.229
    310550_232370285in
    v
    GRCh37.p13First PassNC_000001.10Chr1229,310,550232,370,285

    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)
    nssv18250315<0.0013435432
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