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nsv7059899

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,739

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 33 studies. See in: genome view    
    Submitted genomic12,654,321-12,679,059Question Mark
    Overlapping variant regions from other studies: 134 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):12,748,178-12,772,916Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059899Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1612,654,32112,679,059
    nsv7059899RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1612,748,17812,772,916

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756841inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756841Submitted genomicNC_000016.10:g.126
    54321_12679059inv
    GRCh38 (hg38)NC_000016.10Chr1612,654,32112,679,059
    nssv18756841RemappedPerfectNC_000016.9:g.1274
    8178_12772916inv
    GRCh37.p13First PassNC_000016.9Chr1612,748,17812,772,916

    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)
    nssv187568414e-061276268
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