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nsv6708675

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:605

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 66 SVs from 19 studies. See in: genome view    
    Submitted genomic30,782,057-30,782,661Question Mark
    Overlapping variant regions from other studies: 66 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):30,823,549-30,824,153Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6708675Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr330,782,05730,782,661
    nsv6708675RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr330,823,54930,824,153

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18675706duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18675706Submitted genomicNC_000003.12:g.307
    82057_30782661dup
    GRCh38 (hg38)NC_000003.12Chr330,782,05730,782,661
    nssv18675706RemappedPerfectNC_000003.11:g.308
    23549_30824153dup
    GRCh37.p13First PassNC_000003.11Chr330,823,54930,824,153

    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)
    nssv186757064e-061251694
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