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nsv6990801

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,919

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 24 studies. See in: genome view    
    Submitted genomic50,146,491-50,151,409Question Mark
    Overlapping variant regions from other studies: 101 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):50,180,402-50,185,320Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990801Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1650,146,49150,151,409
    nsv6990801RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1650,180,40250,185,320

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624321duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624321Submitted genomicNC_000016.10:g.501
    46491_50151409dup
    GRCh38 (hg38)NC_000016.10Chr1650,146,49150,151,409
    nssv18624321RemappedPerfectNC_000016.9:g.5018
    0402_50185320dup
    GRCh37.p13First PassNC_000016.9Chr1650,180,40250,185,320

    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)
    nssv186243214e-061272912
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