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nsv7054455

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,023

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 22 studies. See in: genome view    
    Submitted genomic49,984,602-49,986,624Question Mark
    Overlapping variant regions from other studies: 135 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):50,211,740-50,213,762Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054455Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr249,984,60249,986,624
    nsv7054455RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr250,211,74050,213,762

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768875inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768875Submitted genomicNC_000002.12:g.499
    84602_49986624inv
    GRCh38 (hg38)NC_000002.12Chr249,984,60249,986,624
    nssv18768875RemappedPerfectNC_000002.11:g.502
    11740_50213762inv
    GRCh37.p13First PassNC_000002.11Chr250,211,74050,213,762

    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)
    nssv187688757e-062276268
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