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nsv7035993

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:664

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 14 studies. See in: genome view    
    Submitted genomic48,728,117-48,728,780Question Mark
    Overlapping variant regions from other studies: 95 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):47,344,654-47,345,317Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7035993Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2048,728,11748,728,780
    nsv7035993RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2047,344,65447,345,317

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18641580duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18641580Submitted genomicNC_000020.11:g.487
    28117_48728780dup
    GRCh38 (hg38)NC_000020.11Chr2048,728,11748,728,780
    nssv18641580RemappedPerfectNC_000020.10:g.473
    44654_47345317dup
    GRCh37.p13First PassNC_000020.10Chr2047,344,65447,345,317

    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)
    nssv186415803.3e-058240170
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