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nsv6324148

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 36 studies. See in: genome view    
    Submitted genomic33,319,801-33,321,200Question Mark
    Overlapping variant regions from other studies: 114 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):33,785,402-33,786,801Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6324148Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr133,319,80133,321,200
    nsv6324148RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr133,785,40233,786,801

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18060966deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18060966Submitted genomicNC_000001.11:g.333
    19801_33321200del
    GRCh38 (hg38)NC_000001.11Chr133,319,80133,321,200
    nssv18060966RemappedPerfectNC_000001.10:g.337
    85402_33786801del
    GRCh37.p13First PassNC_000001.10Chr133,785,40233,786,801

    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)
    nssv180609660.01142938672
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