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nsv6960520

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:540,446

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1489 SVs from 78 studies. See in: genome view    
    Submitted genomic64,700,079-65,240,524Question Mark
    Overlapping variant regions from other studies: 1489 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):65,166,797-65,707,242Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6960520Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,700,07965,240,524
    nsv6960520RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,166,79765,707,242

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18614579duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18614579Submitted genomicNC_000014.9:g.6470
    0079_65240524dup
    GRCh38 (hg38)NC_000014.9Chr1464,700,07965,240,524
    nssv18614579RemappedPerfectNC_000014.8:g.6516
    6797_65707242dup
    GRCh37.p13First PassNC_000014.8Chr1465,166,79765,707,242

    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)
    nssv186145794e-061260840
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