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nsv6650981

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:117

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 23 studies. See in: genome view    
    Submitted genomic48,742,456-48,742,572Question Mark
    Overlapping variant regions from other studies: 115 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):49,208,128-49,208,244Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6650981Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr148,742,45648,742,572
    nsv6650981RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr149,208,12849,208,244

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628340duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628340Submitted genomicNC_000001.11:g.487
    42456_48742572dup
    GRCh38 (hg38)NC_000001.11Chr148,742,45648,742,572
    nssv18628340RemappedPerfectNC_000001.10:g.492
    08128_49208244dup
    GRCh37.p13First PassNC_000001.10Chr149,208,12849,208,244

    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)
    nssv186283404e-061225498
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