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nsv6533720

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,889

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 18 studies. See in: genome view    
    Submitted genomic36,757,304-36,760,192Question Mark
    Overlapping variant regions from other studies: 118 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):35,385,707-35,388,595Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6533720Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2036,757,30436,760,192
    nsv6533720RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2035,385,70735,388,595

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18068067deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18068067Submitted genomicNC_000020.11:g.367
    57304_36760192del
    GRCh38 (hg38)NC_000020.11Chr2036,757,30436,760,192
    nssv18068067RemappedPerfectNC_000020.10:g.353
    85707_35388595del
    GRCh37.p13First PassNC_000020.10Chr2035,385,70735,388,595

    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)
    nssv18068067<0.001138600
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