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nsv6948128

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,606

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 36 studies. See in: genome view    
    Submitted genomic35,117,284-35,119,889Question Mark
    Overlapping variant regions from other studies: 165 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):35,586,490-35,589,095Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6948128Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1435,117,28435,119,889
    nsv6948128RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1435,586,49035,589,095

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18385575deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18385575Submitted genomicNC_000014.9:g.3511
    7284_35119889del
    GRCh38 (hg38)NC_000014.9Chr1435,117,28435,119,889
    nssv18385575RemappedPerfectNC_000014.8:g.3558
    6490_35589095del
    GRCh37.p13First PassNC_000014.8Chr1435,586,49035,589,095

    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)
    nssv183855754e-061275756
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