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nsv6552437

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,415,975

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4088 SVs from 110 studies. See in: genome view    
    Submitted genomic130,128,480-131,544,454Question Mark
    Overlapping variant regions from other studies: 4088 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):130,886,053-132,302,027Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6552437Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2130,128,480131,544,454
    nsv6552437RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2130,886,053132,302,027

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18255225inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18255225Submitted genomicNC_000002.12:g.130
    128480_131544454in
    v
    GRCh38 (hg38)NC_000002.12Chr2130,128,480131,544,454
    nssv18255225RemappedPerfectNC_000002.11:g.130
    886053_132302027in
    v
    GRCh37.p13First PassNC_000002.11Chr2130,886,053132,302,027

    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)
    nssv18255225<0.001737882
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