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nsv6907278

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,085

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view    
    Submitted genomic33,657,570-33,661,654Question Mark
    Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):33,679,116-33,683,200Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6907278Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1133,657,57033,661,654
    nsv6907278RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1133,679,11633,683,200

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18349044deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18349044Submitted genomicNC_000011.10:g.336
    57570_33661654del
    GRCh38 (hg38)NC_000011.10Chr1133,657,57033,661,654
    nssv18349044RemappedPerfectNC_000011.9:g.3367
    9116_33683200del
    GRCh37.p13First PassNC_000011.9Chr1133,679,11633,683,200

    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)
    nssv183490441.1e-053276246
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