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nsv6653798

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 31 studies. See in: genome view    
    Submitted genomic70,228,401-70,235,600Question Mark
    Overlapping variant regions from other studies: 148 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):70,694,084-70,701,283Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6653798Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr170,228,40170,235,600
    nsv6653798RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr170,694,08470,701,283

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18630010duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18630010Submitted genomicNC_000001.11:g.702
    28401_70235600dup
    GRCh38 (hg38)NC_000001.11Chr170,228,40170,235,600
    nssv18630010RemappedPerfectNC_000001.10:g.706
    94084_70701283dup
    GRCh37.p13First PassNC_000001.10Chr170,694,08470,701,283

    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)
    nssv186300104e-061274240
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