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nsv6896843

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,674

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 21 studies. See in: genome view    
    Submitted genomic50,436,915-50,441,588Question Mark
    Overlapping variant regions from other studies: 100 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):52,196,675-52,201,348Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6896843Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,436,91550,441,588
    nsv6896843RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1052,196,67552,201,348

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18336843deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18336843Submitted genomicNC_000010.11:g.504
    36915_50441588del
    GRCh38 (hg38)NC_000010.11Chr1050,436,91550,441,588
    nssv18336843RemappedPerfectNC_000010.10:g.521
    96675_52201348del
    GRCh37.p13First PassNC_000010.10Chr1052,196,67552,201,348

    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)
    nssv183368434e-061275762
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