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nsv7056410

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,136,867

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11728 SVs from 115 studies. See in: genome view    
    Submitted genomic155,671,571-160,808,437Question Mark
    Overlapping variant regions from other studies: 11728 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):156,528,083-161,664,948Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056410Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2155,671,571160,808,437
    nsv7056410RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2156,528,083161,664,948

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766024inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766024Submitted genomicNC_000002.12:g.155
    671571_160808437in
    v
    GRCh38 (hg38)NC_000002.12Chr2155,671,571160,808,437
    nssv18766024RemappedPerfectNC_000002.11:g.156
    528083_161664948in
    v
    GRCh37.p13First PassNC_000002.11Chr2156,528,083161,664,948

    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)
    nssv18766024<0.00143269898
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