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nsv6961277

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,817

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 232 SVs from 56 studies. See in: genome view    
    Submitted genomic3,208,232-3,218,048Question Mark
    Overlapping variant regions from other studies: 232 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):3,258,232-3,268,048Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961277Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,208,2323,218,048
    nsv6961277RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,258,2323,268,048

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400548deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400548Submitted genomicNC_000016.10:g.320
    8232_3218048del
    GRCh38 (hg38)NC_000016.10Chr163,208,2323,218,048
    nssv18400548RemappedPerfectNC_000016.9:g.3258
    232_3268048del
    GRCh37.p13First PassNC_000016.9Chr163,258,2323,268,048

    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)
    nssv184005484e-061275902
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