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nsv7054209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,438

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 303 SVs from 56 studies. See in: genome view    
    Submitted genomic179,637,658-179,660,095Question Mark
    Overlapping variant regions from other studies: 303 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):179,064,659-179,087,096Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5179,637,658179,660,095
    nsv7054209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,064,659179,087,096

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775912inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775912Submitted genomicNC_000005.10:g.179
    637658_179660095in
    v
    GRCh38 (hg38)NC_000005.10Chr5179,637,658179,660,095
    nssv18775912RemappedPerfectNC_000005.9:g.1790
    64659_179087096inv
    GRCh37.p13First PassNC_000005.9Chr5179,064,659179,087,096

    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)
    nssv187759120.0154236270284
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