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nsv6672004

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,401

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 182 SVs from 29 studies. See in: genome view    
    Submitted genomic43,785,555-43,804,955Question Mark
    Overlapping variant regions from other studies: 182 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):44,012,694-44,032,094Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6672004Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr243,785,55543,804,955
    nsv6672004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr244,012,69444,032,094

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18465074deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18465074Submitted genomicNC_000002.12:g.437
    85555_43804955del
    GRCh38 (hg38)NC_000002.12Chr243,785,55543,804,955
    nssv18465074RemappedPerfectNC_000002.11:g.440
    12694_44032094del
    GRCh37.p13First PassNC_000002.11Chr244,012,69444,032,094

    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)
    nssv184650744e-061276162
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