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nsv6990398

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:82,209

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 317 SVs from 53 studies. See in: genome view    
    Submitted genomic60,076,885-60,159,093Question Mark
    Overlapping variant regions from other studies: 317 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):58,154,246-58,236,454Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990398Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1760,076,88560,159,093
    nsv6990398RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1758,154,24658,236,454

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627996duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627996Submitted genomicNC_000017.11:g.600
    76885_60159093dup
    GRCh38 (hg38)NC_000017.11Chr1760,076,88560,159,093
    nssv18627996RemappedPerfectNC_000017.10:g.581
    54246_58236454dup
    GRCh37.p13First PassNC_000017.10Chr1758,154,24658,236,454

    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)
    nssv186279964e-061275842
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