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nsv7077118

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 16 studies. See in: genome view    
    Submitted genomic29,768,510-29,768,588Question Mark
    Overlapping variant regions from other studies: 83 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):30,342,647-30,342,725Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077118Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1329,768,51029,768,588
    nsv7077118RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1330,342,64730,342,725

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752277inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752277Submitted genomicNC_000013.11:g.297
    68510_29768588inv
    GRCh38 (hg38)NC_000013.11Chr1329,768,51029,768,588
    nssv18752277RemappedPerfectNC_000013.10:g.303
    42647_30342725inv
    GRCh37.p13First PassNC_000013.10Chr1330,342,64730,342,725

    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)
    nssv18752277<0.001164274706
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