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nsv7011043

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,216

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 320 SVs from 31 studies. See in: genome view    
    Submitted genomic63,643,684-63,645,899Question Mark
    Overlapping variant regions from other studies: 320 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):61,310,918-61,313,133Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7011043Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1863,643,68463,645,899
    nsv7011043RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1861,310,91861,313,133

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18418787deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18418787Submitted genomicNC_000018.10:g.636
    43684_63645899del
    GRCh38 (hg38)NC_000018.10Chr1863,643,68463,645,899
    nssv18418787RemappedPerfectNC_000018.9:g.6131
    0918_61313133del
    GRCh37.p13First PassNC_000018.9Chr1861,310,91861,313,133

    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)
    nssv18418787<0.001101266542
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