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nsv6873137

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,559

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 447 SVs from 36 studies. See in: genome view    
    Submitted genomic2,608,036-2,653,594Question Mark
    Overlapping variant regions from other studies: 449 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):2,608,036-2,653,594Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6873137Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr92,608,0362,653,594
    nsv6873137RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr92,608,0362,653,594

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18566061deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18566061Submitted genomicNC_000009.12:g.260
    8036_2653594del
    GRCh38 (hg38)NC_000009.12Chr92,608,0362,653,594
    nssv18566061RemappedPerfectNC_000009.11:g.260
    8036_2653594del
    GRCh37.p13First PassNC_000009.11Chr92,608,0362,653,594

    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)
    nssv185660614e-061276256
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