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nsv7000130

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:365

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 17 studies. See in: genome view    
    Submitted genomic50,902,683-50,903,047Question Mark
    Overlapping variant regions from other studies: 169 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):48,429,053-48,429,417Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7000130Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1850,902,68350,903,047
    nsv7000130RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1848,429,05348,429,417

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18632678duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18632678Submitted genomicNC_000018.10:g.509
    02683_50903047dup
    GRCh38 (hg38)NC_000018.10Chr1850,902,68350,903,047
    nssv18632678RemappedPerfectNC_000018.9:g.4842
    9053_48429417dup
    GRCh37.p13First PassNC_000018.9Chr1848,429,05348,429,417

    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)
    nssv186326786.4e-0516243170
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