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nsv6806487

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,651

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 17 studies. See in: genome view    
    Submitted genomic139,980,523-139,983,173Question Mark
    Overlapping variant regions from other studies: 94 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):140,301,660-140,304,310Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6806487Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6139,980,523139,983,173
    nsv6806487RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6140,301,660140,304,310

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18519116deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18519116Submitted genomicNC_000006.12:g.139
    980523_139983173de
    l
    GRCh38 (hg38)NC_000006.12Chr6139,980,523139,983,173
    nssv18519116RemappedPerfectNC_000006.11:g.140
    301660_140304310de
    l
    GRCh37.p13First PassNC_000006.11Chr6140,301,660140,304,310

    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)
    nssv18519116<0.00136275392
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