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nsv6847362

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:203,578

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 650 SVs from 62 studies. See in: genome view    
    Submitted genomic98,091,407-98,294,984Question Mark
    Overlapping variant regions from other studies: 650 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):99,103,635-99,307,212Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6847362Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr898,091,40798,294,984
    nsv6847362RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr899,103,63599,307,212

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738945duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738945Submitted genomicNC_000008.11:g.980
    91407_98294984dup
    GRCh38 (hg38)NC_000008.11Chr898,091,40798,294,984
    nssv18738945RemappedPerfectNC_000008.10:g.991
    03635_99307212dup
    GRCh37.p13First PassNC_000008.10Chr899,103,63599,307,212

    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)
    nssv187389454e-061276056
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