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nsv7000006

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 44 studies. See in: genome view    
    Submitted genomic21,132,001-21,141,700Question Mark
    Overlapping variant regions from other studies: 165 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):21,314,804-21,324,503Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7000006Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1921,132,00121,141,700
    nsv7000006RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1921,314,80421,324,503

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18422605deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18422605Submitted genomicNC_000019.10:g.211
    32001_21141700del
    GRCh38 (hg38)NC_000019.10Chr1921,132,00121,141,700
    nssv18422605RemappedPerfectNC_000019.9:g.2131
    4804_21324503del
    GRCh37.p13First PassNC_000019.9Chr1921,314,80421,324,503

    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)
    nssv18422605<0.00131275984
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