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nsv6721503

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,952

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 197 SVs from 44 studies. See in: genome view    
    Submitted genomic15,783,841-15,799,792Question Mark
    Overlapping variant regions from other studies: 197 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):15,785,464-15,801,415Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6721503Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr415,783,84115,799,792
    nsv6721503RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr415,785,46415,801,415

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18491901deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18491901Submitted genomicNC_000004.12:g.157
    83841_15799792del
    GRCh38 (hg38)NC_000004.12Chr415,783,84115,799,792
    nssv18491901RemappedPerfectNC_000004.11:g.157
    85464_15801415del
    GRCh37.p13First PassNC_000004.11Chr415,785,46415,801,415

    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)
    nssv184919014e-061275938
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