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nsv6661680

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:356,863

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1148 SVs from 79 studies. See in: genome view    
    Submitted genomic241,326,577-241,683,439Question Mark
    Overlapping variant regions from other studies: 1151 SVs from 79 studies. See in: genome view    
    Remapped(Score: Good):241,489,877-241,846,741Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6661680Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1241,326,577241,683,439
    nsv6661680RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1241,489,877241,846,741

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18610088duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18610088Submitted genomicNC_000001.11:g.241
    326577_241683439du
    p
    GRCh38 (hg38)NC_000001.11Chr1241,326,577241,683,439
    nssv18610088RemappedGoodNC_000001.10:g.241
    489877_241846741du
    p
    GRCh37.p13First PassNC_000001.10Chr1241,489,877241,846,741

    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)
    nssv186100884e-061275486
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