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nsv6994515

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 19 studies. See in: genome view    
    Submitted genomic65,557,201-65,559,400Question Mark
    Overlapping variant regions from other studies: 82 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):65,591,104-65,593,303Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6994515Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1665,557,20165,559,400
    nsv6994515RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1665,591,10465,593,303

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18401808deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18401808Submitted genomicNC_000016.10:g.655
    57201_65559400del
    GRCh38 (hg38)NC_000016.10Chr1665,557,20165,559,400
    nssv18401808RemappedPerfectNC_000016.9:g.6559
    1104_65593303del
    GRCh37.p13First PassNC_000016.9Chr1665,591,10465,593,303

    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)
    nssv184018084e-061254974
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