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nsv6815695

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:301,488

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 827 SVs from 64 studies. See in: genome view    
    Submitted genomic106,124,034-106,425,521Question Mark
    Overlapping variant regions from other studies: 827 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):106,571,909-106,873,396Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6815695Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6106,124,034106,425,521
    nsv6815695RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6106,571,909106,873,396

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18708834duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18708834Submitted genomicNC_000006.12:g.106
    124034_106425521du
    p
    GRCh38 (hg38)NC_000006.12Chr6106,124,034106,425,521
    nssv18708834RemappedPerfectNC_000006.11:g.106
    571909_106873396du
    p
    GRCh37.p13First PassNC_000006.11Chr6106,571,909106,873,396

    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)
    nssv187088344e-061276004
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