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nsv6548767

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:505

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 14 studies. See in: genome view    
    Submitted genomic200,893,898-200,894,402Question Mark
    Overlapping variant regions from other studies: 125 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):201,758,621-201,759,125Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6548767Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2200,893,898200,894,402
    nsv6548767RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2201,758,621201,759,125

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256359inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256359Submitted genomicNC_000002.12:g.200
    893898_200894402in
    v
    GRCh38 (hg38)NC_000002.12Chr2200,893,898200,894,402
    nssv18256359RemappedPerfectNC_000002.11:g.201
    758621_201759125in
    v
    GRCh37.p13First PassNC_000002.11Chr2201,758,621201,759,125

    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)
    nssv18256359<0.001134528
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