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nsv6711933

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,086

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 267 SVs from 43 studies. See in: genome view    
    Submitted genomic121,362,664-121,448,749Question Mark
    Overlapping variant regions from other studies: 267 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):121,081,511-121,167,596Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6711933Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3121,362,664121,448,749
    nsv6711933RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3121,081,511121,167,596

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18670605duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18670605Submitted genomicNC_000003.12:g.121
    362664_121448749du
    p
    GRCh38 (hg38)NC_000003.12Chr3121,362,664121,448,749
    nssv18670605RemappedPerfectNC_000003.11:g.121
    081511_121167596du
    p
    GRCh37.p13First PassNC_000003.11Chr3121,081,511121,167,596

    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)
    nssv186706053.6e-0510274832
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