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nsv6736047

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,419

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 21 studies. See in: genome view    
    Submitted genomic172,264,776-172,267,194Question Mark
    Overlapping variant regions from other studies: 99 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):171,982,566-171,984,984Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6736047Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3172,264,776172,267,194
    nsv6736047RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3171,982,566171,984,984

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18476414deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18476414Submitted genomicNC_000003.12:g.172
    264776_172267194de
    l
    GRCh38 (hg38)NC_000003.12Chr3172,264,776172,267,194
    nssv18476414RemappedPerfectNC_000003.11:g.171
    982566_171984984de
    l
    GRCh37.p13First PassNC_000003.11Chr3171,982,566171,984,984

    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)
    nssv184764143.6e-0510274918
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