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nsv6657960

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,611

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 29 studies. See in: genome view    
    Submitted genomic99,070,506-99,073,116Question Mark
    Overlapping variant regions from other studies: 129 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):99,536,062-99,538,672Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6657960Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr199,070,50699,073,116
    nsv6657960RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr199,536,06299,538,672

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18429081deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18429081Submitted genomicNC_000001.11:g.990
    70506_99073116del
    GRCh38 (hg38)NC_000001.11Chr199,070,50699,073,116
    nssv18429081RemappedPerfectNC_000001.10:g.995
    36062_99538672del
    GRCh37.p13First PassNC_000001.10Chr199,536,06299,538,672

    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)
    nssv18429081<0.00132275440
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