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nsv7052037

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,136,429

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3006 SVs from 89 studies. See in: genome view    
    Submitted genomic69,732,002-70,868,430Question Mark
    Overlapping variant regions from other studies: 2035 SVs from 80 studies. See in: genome view    
    Remapped(Score: Pass):69,959,134-70,660,850Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052037Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr269,732,00270,868,430
    nsv7052037RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr269,959,13470,660,850

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769619inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769619Submitted genomicNC_000002.12:g.697
    32002_70868430inv
    GRCh38 (hg38)NC_000002.12Chr269,732,00270,868,430
    nssv18769619RemappedPassNC_000002.11:g.699
    59134_70660850inv
    GRCh37.p13First PassNC_000002.11Chr269,959,13470,660,850

    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)
    nssv18769619<0.001236274256
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