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nsv7012907

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:191

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 79 SVs from 20 studies. See in: genome view    
    Submitted genomic6,494,502-6,494,692Question Mark
    Overlapping variant regions from other studies: 79 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):6,494,513-6,494,703Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7012907Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr196,494,5026,494,692
    nsv7012907RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr196,494,5136,494,703

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18424556deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18424556Submitted genomicNC_000019.10:g.649
    4502_6494692del
    GRCh38 (hg38)NC_000019.10Chr196,494,5026,494,692
    nssv18424556RemappedPerfectNC_000019.9:g.6494
    513_6494703del
    GRCh37.p13First PassNC_000019.9Chr196,494,5136,494,703

    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)
    nssv184245560.004975229764
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