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nsv6707788

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 33 studies. See in: genome view    
    Submitted genomic47,211,327-47,211,362Question Mark
    Overlapping variant regions from other studies: 119 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):47,252,817-47,252,852Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6707788Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr347,211,32747,211,362
    nsv6707788RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr347,252,81747,252,852

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18482763deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18482763Submitted genomicNC_000003.12:g.472
    11327_47211362del
    GRCh38 (hg38)NC_000003.12Chr347,211,32747,211,362
    nssv18482763RemappedPerfectNC_000003.11:g.472
    52817_47252852del
    GRCh37.p13First PassNC_000003.11Chr347,252,81747,252,852

    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)
    nssv184827631.6e-054246338
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