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nsv6789580

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,961

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 33 studies. See in: genome view    
    Submitted genomic56,974,142-57,019,102Question Mark
    Overlapping variant regions from other studies: 174 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):56,838,940-56,883,900Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6789580Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr656,974,14257,019,102
    nsv6789580RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr656,838,94056,883,900

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715677duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715677Submitted genomicNC_000006.12:g.569
    74142_57019102dup
    GRCh38 (hg38)NC_000006.12Chr656,974,14257,019,102
    nssv18715677RemappedPerfectNC_000006.11:g.568
    38940_56883900dup
    GRCh37.p13First PassNC_000006.11Chr656,838,94056,883,900

    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)
    nssv187156774e-061275684
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