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nsv6705353

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:119,225

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 346 SVs from 55 studies. See in: genome view    
    Submitted genomic63,756,717-63,875,941Question Mark
    Overlapping variant regions from other studies: 346 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):63,742,393-63,861,617Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6705353Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr363,756,71763,875,941
    nsv6705353RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr363,742,39363,861,617

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18678108duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18678108Submitted genomicNC_000003.12:g.637
    56717_63875941dup
    GRCh38 (hg38)NC_000003.12Chr363,756,71763,875,941
    nssv18678108RemappedPerfectNC_000003.11:g.637
    42393_63861617dup
    GRCh37.p13First PassNC_000003.11Chr363,742,39363,861,617

    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)
    nssv186781084e-061272774
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