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nsv6973985

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,754

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157 SVs from 26 studies. See in: genome view    
    Submitted genomic48,814,737-48,848,490Question Mark
    Overlapping variant regions from other studies: 157 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):49,106,934-49,140,687Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6973985Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1548,814,73748,848,490
    nsv6973985RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1549,106,93449,140,687

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18394021deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18394021Submitted genomicNC_000015.10:g.488
    14737_48848490del
    GRCh38 (hg38)NC_000015.10Chr1548,814,73748,848,490
    nssv18394021RemappedPerfectNC_000015.9:g.4910
    6934_49140687del
    GRCh37.p13First PassNC_000015.9Chr1549,106,93449,140,687

    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)
    nssv183940214e-061276224
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