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nsv7047206

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:457,999

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2944 SVs from 110 studies. See in: genome view    
    Submitted genomic248,129,213-248,587,211Question Mark
    Overlapping variant regions from other studies: 2947 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):248,292,515-248,750,512Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047206Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1248,129,213248,587,211
    nsv7047206RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1248,292,515248,750,512

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760139inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760139Submitted genomicNC_000001.11:g.248
    129213_248587211in
    v
    GRCh38 (hg38)NC_000001.11Chr1248,129,213248,587,211
    nssv18760139RemappedPerfectNC_000001.10:g.248
    292515_248750512in
    v
    GRCh37.p13First PassNC_000001.10Chr1248,292,515248,750,512

    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)
    nssv187601390.002590274978
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